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	<title>CeliacNurse &#187; 12 Part Series: CD Symptoms</title>
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	<description>Tips for the Gluten-Free Community</description>
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		<title>Part 12 Of 12 Part Series: Celiac Disease Symptom Checklist</title>
		<link>http://celiacnurse.com/part-12-of-12-part-series-celiac-disease-symptom-checklist/</link>
		<comments>http://celiacnurse.com/part-12-of-12-part-series-celiac-disease-symptom-checklist/#comments</comments>
		<pubDate>Thu, 03 Dec 2009 06:45:12 +0000</pubDate>
		<dc:creator>Shelly</dc:creator>
				<category><![CDATA[12 Part Series: CD Symptoms]]></category>

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		<description><![CDATA[This is the twelfth post in the 12 part series discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, a list of CD symptoms is included in a PDF format. As you review the symptoms, keep in mind that some individuals will only have one or two [...]]]></description>
			<content:encoded><![CDATA[<p>This is the twelfth post in the 12 part series discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, a list of CD symptoms is included in a PDF format. As you review the symptoms, keep in mind that some individuals will only have one or two symptoms (for example, anemia and night blindness) and others may have many symptoms. Celiac Disease can be quite elusive, which makes it difficult to diagnose. </p>
<p><a href="http://www.celiacnurse.com/wp-content/uploads/2009/12/Celiac_Disease_Symptom_Checklist.pdf">“Celiac Disease Symptom Checklist”</a></p>
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		<title>Part 11 of 12 Part Series: List of Diseases/Syndromes Associated With Celiac Disease</title>
		<link>http://celiacnurse.com/part-11-of-12-part-series-list-of-diseasessyndromes-associated-with-celiac-disease/</link>
		<comments>http://celiacnurse.com/part-11-of-12-part-series-list-of-diseasessyndromes-associated-with-celiac-disease/#comments</comments>
		<pubDate>Tue, 01 Dec 2009 19:08:10 +0000</pubDate>
		<dc:creator>Shelly</dc:creator>
				<category><![CDATA[12 Part Series: CD Symptoms]]></category>

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		<description><![CDATA[This is the eleventh in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, a list of associated diseases/syndromes will be included. Individuals with Celiac Disease have a higher risk of developing other autoimmune diseases. This may be due to genetic influences or [...]]]></description>
			<content:encoded><![CDATA[<p>This is the eleventh in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, a list of associated diseases/syndromes will be included. Individuals with Celiac Disease have a higher risk of developing other autoimmune diseases. This may be due to genetic influences or the heightened permeability of the intestine may allow other environmental antigens access to the immune system. This could lead to an autoimmune response that triggers the development of other autoimmune diseases (5,69). Delayed diagnosis appears to increase the risk as well. Therefore, early recognition and diagnosis is important for primary prevention.</p>
<p><span id="more-321"></span></p>
<h3>List of Associated Diseases And Syndromes </h3>
<p>Hashimoto’s Disease (Hypothyroidism) (1-5)</p>
<p>Grave’s Disease (Hyperthyroidism) (1-5)</p>
<p>Type 1 Diabetes (insulin dependent) (1-5,43)</p>
<p>Addison’s Disease (1,6,8)</p>
<p>Primary Biliary Cirrhosis (1,9-13)</p>
<p>Down’s Syndrome (1,4,)</p>
<p>Turner Syndrome (1)</p>
<p>William’s Syndrome (1)</p>
<p>Primary Adrenal Insufficiency (7,72)</p>
<p>IgA Nephropathy (44,45)</p>
<p>IgA Deficiency (1)</p>
<p>Alopecia Areata (1)</p>
<p>Sjögren’s Syndrome (1,42)</p>
<p>Cardiomyopathy (1,55-60)</p>
<p>Malignancy (1)</p>
<p>Vasculitis (18,63)</p>
<p>Antiphospholipid Syndrome (17,33,61,62)</p>
<p>Thrombocytopenic Purpura (ITP) (67,68)</p>
<p>Systemic Sclerosis (19)</p>
<p>Some individuals may be misdiagnosed with systemic lupus erythematosus (1,4,14-17,70,71), fibromyalgia (1), or polymyalgia rheumatica (1) since these diseases have similar symptoms. Others may only have their&#160; CD symptoms diagnosed as irritable bowel (1-4), lactose intolerance (1,3,4,20), arthritis (1,35-39), miscarriages, infertility (1,4,21-25), osteoporosis (1-4,40,41), aphthous stomatitis (1-4), anemia (1-4), failure to thrive (1-4), various skin rashes (1-4,18), ataxia (1,26-32), epilepsy (1,26-32), and/or myopathies (34,46-54). There are many other possible symptoms and diseases with similar symptoms that are discussed in the 12 part series.&#160; </p>
<p>&#160;<strong>I </strong><strong>recommend waiting until CD/gluten sensitivity testing is complete before initiating a gluten-free diet because it may create a false negative. If your CD test is negative, you may still have a gluten sensitivity. Discuss this with your MD or specialist. </strong><strong>Review your symptoms and everything in this post with a Medical Doctor</strong> <strong>and your specialists before you make any changes</strong>. <strong>Your MD knows your medical history and the treatments that are appropriate for you.</strong></p>
<dt>
<p><strong>References</strong></p>
</dt>
<dt>
<h3><strong></strong></h3>
</dt>
<dt></dt>
<dt>
<p>1. <cite><strong>Excellent Book:</strong> Green PHR, Jones, R. Celiac Disease A Hidden Epidemic. Collins, Harper Collins Publishers, 2006 <b><a href="http://tinyurl.com/ljeqjc">http://tinyurl.com/ljeqjc</a> </b></cite></p>
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<p><cite></cite><cite>2. </cite>Pruessner Harold T, MD. Detecting Celiac Disease In Your Patients. American Family Physician. March 1st, 1998.</p>
</dt>
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<p>3. Feldman Mark, MD, Friedman Lawrence S, MD, Sleisenger, Marvin H, MD, Gastrointestinal and Liver Disease Pathophysiology/Diagnosis/Management 7th Edition, Volume11, 2002,Saunders</p>
</dt>
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<p>4. Celiac Disease <a title="http://www.nlm.nih.gov/medlineplus/ency/article/000233.htm" href="http://www.nlm.nih.gov/medlineplus/ency/article/000233.htm">http://www.nlm.nih.gov/medlineplus/ency/article/000233.htm</a> </p>
</dt>
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<p>5. Alessio Fasano<strong>.</strong> Systemic Autoimmune Disorders in Celiac Disease: Autoimmune Diseases Associated with Celiac Disease. <a title="http://www.medscape.com/viewarticle/547107_4" href="http://www.medscape.com/viewarticle/547107_4">http://www.medscape.com/viewarticle/547107_4</a></p>
</dt>
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<p>6. C. O&#8217;leary, C.H. Walsh, P. Wieneke, P. O&#8217;regan, B. Buckley, D.J. O&#8217;halloran, J.B. Ferriss, E.M.M. Quigley, P. Annis, F. Shanahan<a name="RFN1"></a><sup><a href="http://qjmed.oxfordjournals.org/cgi/content/full/95/2/79#FN1"></a></sup> and C.C. Cronin. Coeliac disease and autoimmune Addison&#8217;s disease: a clinical pitfall. Q J Med 2002; <b>95</b>: 79-82.</p>
</dt>
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<p>7. Elfström et al. Risk of primary adrenal insufficiency in patients with celiac disease. <em>J Clin Endocrinol Metab .</em>2007</p>
</dt>
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<p>8. Corrado Betterle<sup></sup>, Francesca Lazzarotto<sup></sup>, Aglaura Cinzia Spadaccino<sup></sup>, Daniela Basso<sup>1</sup>, Mario Plebani<sup>1</sup>, Beniamino Pedini<sup></sup>, Silvia Chiarelli<sup>2</sup> and Mariapaola Albergoni<sup>3</sup> Celiac disease in North Italian patients with autoimmune Addison’s disease. European Journal of Endocrinology, Vol 154, Issue 2, 275-279</p>
</dt>
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<p>9. <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Logan%20RF%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Logan RF</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Ferguson%20A%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Ferguson A</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Finlayson%20ND%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Finlayson ND</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Weir%20DG%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Weir DG</a>. Primary biliary cirrhosis and coeliac disease: an association? <a href="http://www.ncbi.nlm.nih.gov/">Lancet.</a> 1978 Feb 4;1(8058):230-3.</p>
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<p>10. Primary biliary cirrhosis and coeliac disease. Lancet. 1978 Apr 1;1(8066):713–714.11. </p>
</dt>
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<p>11. Shanahan F, O&#8217;Regan PF, Crowe JP. Primary Biliary Cirrhosis associated with Coeliac Disease. Ir Med J. 1983 Jun;76(6):282–282.</p>
</dt>
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<p>12. Schrijver G, Van Berge Henegouwen GP, Bronkhorst FB. Gluten-sensitive coeliac disease and primary biliary cirrhosis syndrome. Neth J Med. 1984;27(6):218–221</p>
</dt>
<dt>
<p>13. P. Ginn and R. D. Workman. Primary biliary cirrhosis and adult celiac disease. West J Med. 1992 May; 156(5): 547–549. </p>
<p>14. Mirza, E. Bonilla and P. E. Phillips. Celiac disease in a patient with systemic lupus erythematosus: a case report and review of literature. Journal <a href="http://www.springerlink.com/content/102818/?p=c013328d2a5549078aae178c14b29bea&amp;pi=0">Clinical Rheumatology</a> Issue <a href="http://www.springerlink.com/content/j37884h434k0/?p=c013328d2a5549078aae178c14b29bea&amp;pi=0">Volume 26, Number 5 / May, 2007</a></p>
</dt>
<dt>
<p>15. Mondher Zitouni, Wafa Daoud, Maryam Kallel and Sondés Makni. Systemic lupus erythematosus with celiac disease: a report of five cases. <a href="http://www.sciencedirect.com/science/journal/1297319X"><b>Joint Bone Spine</b></a>&#160;<a href="http://www.sciencedirect.com/science?_ob=PublicationURL&amp;_tockey=%23TOC%236668%232004%23999289995%23513288%23FLA%23&amp;_cdi=6668&amp;_pubType=J&amp;view=c&amp;_auth=y&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=81f40a2c23b32519aa19377a6b7ffcd3">Volume 71, Issue 4</a>, July 2004, Pages 344-346.</p>
</dt>
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<p>16. <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Freeman%20HJ%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Freeman HJ</a>. Adult celiac disease followed by onset of systemic lupus erythematosus. <a href="http://www.ncbi.nlm.nih.gov/">J Clin Gastroenterol.</a> 2008 Mar;42(3):252-5.</p>
</dt>
<dt>
<p>17. Deepak Gupta and Naureen Mirza<sup>. </sup>Systemic lupus erythematosus, celiac disease and antiphospholipid antibody syndrome: a rare association. Journal <a href="http://www.springerlink.com/content/101577/?p=81c14503467f48f78cce76fdee6a5c1f&amp;pi=0">Rheumatology International</a> Issue <a href="http://www.springerlink.com/content/vjg1r2232580/?p=81c14503467f48f78cce76fdee6a5c1f&amp;pi=0">Volume 28, Number 11 / September, 2008</a></p>
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<dt>
<p>18. Abenavoli L, Proietti I, Leggio L, Ferrulli A, Vonghia L, Capizzi R, Rotoli M, Amerio PL, Gasbarrini g, Addolorato G. Cutaneous Manifestations In Celiac disease. World Journal Of Gastroenterology. 2006 February 14;12(6):843-852</p>
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<p>19. <a href="http://www.jrheum.org/search?author1=EDOARDO+ROSATO&amp;sortspec=date&amp;submit=Submit">EDOARDO ROSATO</a>, <a href="http://www.jrheum.org/search?author1=DANIELA+De+NITTO&amp;sortspec=date&amp;submit=Submit">DANIELA De NITTO</a>, <a href="http://www.jrheum.org/search?author1=CARMELINA+ROSSI&amp;sortspec=date&amp;submit=Submit">CARMELINA ROSSI</a>, <a href="http://www.jrheum.org/search?author1=VALERIO+LIBANORI&amp;sortspec=date&amp;submit=Submit">VALERIO LIBANORI</a>, <a href="http://www.jrheum.org/search?author1=GIUSEPPE+DONATO&amp;sortspec=date&amp;submit=Submit">GIUSEPPE DONATO</a>, <a href="http://www.jrheum.org/search?author1=MARCO+Di+TOLA&amp;sortspec=date&amp;submit=Submit">MARCO Di TOLA</a>, <a href="http://www.jrheum.org/search?author1=SIMONETTA+PISARRI&amp;sortspec=date&amp;submit=Submit">SIMONETTA PISARRI</a>, <a href="http://www.jrheum.org/search?author1=FELICE+SALSANO&amp;sortspec=date&amp;submit=Submit">FELICE SALSANO</a> and <a href="http://www.jrheum.org/search?author1=ANTONIO+PICARELLI&amp;sortspec=date&amp;submit=Submit">ANTONIO PICARELLI</a>. High Incidence of Celiac Disease in Patients with Systemic Sclerosis. The Journal of Rheumatology. <a title="http://www.jrheum.org/content/36/5/965.abstract" href="http://www.jrheum.org/content/36/5/965.abstract">http://www.jrheum.org/content/36/5/965.abstract</a></p>
</dt>
<dt>
<p>20. Melvin B. Heyman, MD. Lactose Intolerance in Infants, Children, and Adolescents. PEDIATRICS Vol. 118 No. 3 September 2006, pp. 1279-1286.</p>
</dt>
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<p>21. ELIAKIM Rami<sup> (1)</sup> ; SHERER David M.<sup> (2)</sup><strong> ; </strong>Celiac disease : Fertility and pregnancy.&#160; <sup>(1) </sup>Division of Gastroenterology, Rambam Medical Center, Technion School of Medicine, Haifa, ISRAEL. <sup>(2) </sup>Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, St. Luke’s-Roosevelt Hospital Center, University of Columbia College of Physicians and Surgeons, New York, N.Y., ETATS-UNIS. <a href="http://cat.inist.fr/?aModele=afficheN&amp;cpsidt=859066">http://cat.inist.fr/?aModele=afficheN&amp;cpsidt=859066</a></p>
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<p>22. A.Gasbarrini, E.Torre, C.Trivellini, S.De Carolis, A.Caruso, G.Gasbarrini. Recurrent spontaneous abortion and intrauterine fetal growth retardation as symptoms of coeliac disease. <em>The Lancet</em>, Volume 356, Issue 9227, Pages 399-400.</p>
</p>
</dt>
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<p>23. Rami Eliakim<sup>a</sup>, David M. Sherer<sup>b</sup> Celiac Disease: Fertility and Pregnancy. <i>Gynecol Obstet Invest</i> 2001;51:3-7.</p>
</p>
</dt>
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<p>20. Porpora, Maria Grazia MD; Picarelli, Antonio MD; Porta, Romana Prosperi MD; Di Tola, Marco BSc; D’Elia, Claudia MD; Cosmi, Ermelando Vinicio MD, PhD.&#160; Celiac Disease as a Cause of Chronic Pelvic Pain, Dysmenorrhea, and Deep Dyspareunia. Obstetrics &amp; Gynecology: May 2002 – Volume 99 – Issue 5, Part 2 – p 937-939.</p>
</p>
</dt>
<dt>
<p>21. P Collin, S Vilska, P K Heinonen, O Hällström, P Pikkarainen. Infertility and coeliac disease. <i>Gut</i> 1996;<b>39</b>:382-384; doi:10.1136/gut.39.3.382.</p>
</p>
</dt>
<dt>
<p>22. K <b>Rostami</b>, EAP Steegers, WY Wong, DD … – Coeliac disease and reproductive disorders: a <strong>neglected</strong> association. European Journal of Obstetrics and Gynecology, 2001 – Elsevier. Science Ireland Ltd. All rights reserved.</p>
</p>
</dt>
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<p>23. <em>Bradley, Ryan J. * and; Rosen, Mitchell P. MD + </em>Subfertility and Gastrointestinal Disease: ‘Unexplained’ Is Often Undiagnosed. Obstetrical &amp; Gynecological Survey. 59(2):108-117, February 2004. </p>
</p>
</dt>
<dt>
<p>24. Gian Mario Tiboni<sup>1</sup><sup>,3</sup>, Maria Grazia de Vita<sup>1</sup>, Raffaella Faricelli<sup>2</sup>, Franca Giampietro<sup>1</sup> and Marco Liberati<sup>1</sup> Serological testing for celiac disease in women undergoing assisted reproduction techniques. Human reproduction Vol 21, No. 2 pp376-379,2206. <a href="http://humrep.oxfordjournals.org/cgi/reprint/21/2/376.pdf">http://humrep.oxfordjournals.org/cgi/reprint/21/2/376.pdf</a></p>
</p>
</dt>
<dt>
<p>25. Adams Scott. Miscarriage: Italian Researchers Link celiac Disease To Spontaneous Abortion And Fetal Growth Retardation. <a href="http://www.celiac.com">www.celiac.com</a> <b><a href="http://tinyurl.com/yaxxj6s">http://tinyurl.com/yaxxj6s</a></b></p>
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<dt>
<p>26. Dickey W. Epilepsy, Cerebral Calcifications, and Coeliac Disease. Lancet 1994;344:1585-6</p>
</p>
</dt>
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<p>27. Gobbi G, Bouquet F, Greco L, et al. Coeliac Disease, Epilepsy, and Cerebral Calcifications. The Italian Working Group On Coeliac Disease and Epilepsy. Lancet 340:439, 1992.</p>
</p>
</dt>
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<p>28. Hadjivassiliou M, Davies-Jones GA, Saunders DS, Grunwald (<strong>2 dots</strong>)RA. Dietary treatment of Gluten Ataxia. J Neuro Neurosurg Psychiatry. 2003 Sep;74(9):1221-4.</p>
</dt>
<dt>
<p>29. Hadjivassiliou M, <em>Grünwald</em> R, Sharrack B, Sanders D, Lobo A, Williamson C, Woodroofe N, Wood N, Davies-Jones A. Gluten Ataxia in Perspective: Epidemiology, Genetic susceptibility, And Clinical Characteristics. Brain 2003 Mar;126(pt 3): 685-91.</p>
<p>30. Hadjivassilou M, <em>Grünwald</em> RA, Lawden M, Davies-Jones GA, Powell T, Smith CM. Headache and CNS White Matter Abnormalties Associated with Gluten Sensitivity. Neurology 2001 Feb 13;56(3):385-8.</p>
<p>31.Cooke WT, Thomas-Smith W. Neurological Disorders Associated with Adult Coeliac Disease. Brain 1966;89:683-722. </p>
<p>32. Hadjivassilou M and <em>Grünwald</em> RA, Davies-Jones GAB. Gluten Sensitivity As a Neurological Illness. Journal of Neurology, Neurosurgery, and Psychiatry 2002;72:560-563</p>
<p>33. <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Jorge%20O%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Jorge O</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Jorge%20A%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Jorge A</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Camus%20G%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Camus G</a>. Celiac disease associated with antiphospholipid syndrome. <a href="http://www.ncbi.nlm.nih.gov/">Rev Esp Enferm Dig.</a> 2008 Feb;100(2):102-3. </p>
</p>
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<p>34. Hall WH. Proximal muscle atrophy in adult celiac disease. Am J Dig Dis. 1968 Aug;13(8):697–704.</p>
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<p>35. Hafström, et el. A Vegan diet free Of gluten Improves The signs And symptoms Of Rheumatoid Arthritis: The Effects on Arthritis correlate With A reduction In Antibodies To Food Antigens. Rheumatology 2001;40:1175-9 </p>
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<p>36. Lubrano et el. The Arthritis of Celiac Disease: Prevalence And Pattern In 200 Adult Patients. British Journal of Rheumatology. 1996;35:1314-8.</p>
</p>
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<p>37. Bourne JT, Kumar P, Huskisson EC, Mageed R, Unsworth DJ, Wojtulewski JA. Arthritis And Celiac disease. Ann Rheum Dis 1985, September;44(9):592-598.</p>
</p>
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<p>38. Adams Jefferson. Studies Show High Instance of Rheumatoid Arthritis And Osteoporosis In Patients With Celiac Disease. <a href="http://www.celiac.com">www.celiac.com</a></p>
</p>
</dt>
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<p>39. Collin P, Korpela M, Hallstrom O, et el. Rheumatic Complaints As A Presenting Symptom In Patients With Celiac Disease. Scan J Rheumatol 1992;21:20-3.</p>
</dt>
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<p>40. Patients With Osteoporosis Should Be Screened For Celiac Disease, Study Suggests. ScienceDaily (Mar. 16, 2005) — St. Louis, Feb. 28, 2005. <a href="http://www.sciencedaily.com/releases/2005/03/050308131921.htm">http://www.sciencedaily.com/releases/2005/03/050308131921.htm</a></p>
</p>
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<p>41. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Stazi%20AV%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Stazi AV</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Trecca%20A%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Trecca A</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Trinti%20B%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Trinti B</b></a>. Osteoporosis in celiac disease and in endocrine and reproductive disorders. <a href="http://www.ncbi.nlm.nih.gov/">World J Gastroenterol.</a> 2008 Jan 28;14(4):498-505.</p>
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<p>42. Szodoray P, Barta Z, Lakos, Szakall S, Zeher M. Coeliac Disease In Sjogren’s Syndrome-A Study of 111 Hungarian Patients. Rheumatol Int 2004 Sep;24(5):278-82. Epub 2003 Sep 17.</p>
<p>43. Matz Jenilee. The Link Between Type 1 Diabetes and Celiac Disease. http:www.myoptumhealth.com</p>
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<dt>
<p>44. Hilde Kloster Smerud, Bengt Fellström, Roger Hällgren, Sonia Osagie, Per Venge and Gudjón Kristjánsson Gluten sensitivity in patients with IgA nephropathy. Nephrology Dialysis Transplantation 2009 24(8):2476-2481; doi:10.1093/ndt/gfp133.</p>
</p>
</dt>
<dt>
<p>45. Pekka Collin, M.D., Jaana Syrjänen, M.D. , Jukka Partanen, Ph.D&#160; , Amos Pasternack, M.D.&#160; , Katri Kaukinen, M.D.&#160; , Jukka Mustonen, M.D. Celiac disease and HLA DQ in patients with IgA nephropathy. T<a href="http://www3.interscience.wiley.com/journal/117955841/home">he American Journal of Gastroenterology</a> <strong><a href="http://www3.interscience.wiley.com/journal/118937069/issue">Volume 97 Issue 10</a>, Pages 2572 – 2576</strong></p>
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<p>46. Sandyk R., MD, Brennan M.J.W., MB, BCh, PhD. Isolated Ocular Myopathy And Celiac Disease In Childhood. Neurology 1983;33:792. American Academy Of Neurology.</p>
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<p>47. Wong M, et el. Proximal Myopathy And Bone Pain As The Presenting Features Of Coeliac Disease. Ann Rheum Dis, 2002, 61(1):p87-8.</p>
<p>48. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Kleopa%20KA%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus">Kleopa KA</a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Kyriacou%20K%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus">Kyriacou K</a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Zamba-Papanicolaou%20E%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus">Zamba-Papanicolaou E</a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Kyriakides%20T%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus">Kyriakides T</a>. Reversible inflammatory and vacuolar myopathy with vitamin E deficiency in celiac disease. <a href="http://www.ncbi.nlm.nih.gov/">Muscle Nerve.</a> 2005 Feb;31(2):260-5.</p>
<p>49. Possible Relationship Between Myopathies And Celiac Disease. ScienceDaily (Feb. 24, 2007) </p>
<p>50. Albert Selva-O’Callaghan, MD, PhD<sup> 1 *</sup>, Francesc Casellas, MD, PhD<sup> 2</sup>, Ines de Torres, MD, PhD<sup> 3</sup>, Eduard Palou, MD, PhD<sup> 4</sup>, Josep M. Grau-Junyent, MD, PhD<sup> 5</sup>, Miquel Vilardell-Tarrés, MD, PhD<sup> 1 </sup><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&amp;cmd=Retrieve&amp;dopt=AbstractPlus&amp;list_uids=16967485&amp;itool=pubmed_DocSum">Celiac disease and antibodies associated with celiac disease in patients with inflammatory myopathy</a>. <a href="http://www3.interscience.wiley.com/journal/32891/home">Muscle &amp; Nerve</a>, <strong><a href="http://www3.interscience.wiley.com/journal/113518454/issue">Volume 35 Issue 1</a>, Pages 49 – 54.</strong><strong>Published Online: </strong>11 Sep 2006</p>
<p>51. Erkan Kozanoglu<sup>1</sup>, Sibel Basaran<sup>1</sup> and M. Kamil Goncu<sup>1. </sup>Proximal myopathy as an unusual presenting feature of celiac disease. Journal <a href="http://www.springerlink.com/content/102818/?p=67bdc6efa0c94181851ab20c64bd6f62&amp;pi=0">Clinical Rheumatology</a>. Issue <a href="http://www.springerlink.com/content/j64057amj92v/?p=67bdc6efa0c94181851ab20c64bd6f62&amp;pi=0">Volume 24, Number 1 / February, 2005</a>. Pages 76-78</p>
<p>52. Vivek Jain<sup>1</sup>, Rajeshwar Reddy Angitii<sup>1</sup>, Surjit Singh<sup>1</sup>, Babu Ram Thapa<sup>2</sup> and Lata Kumar<sup>1&#160; </sup><sup>Proximal Muscle Weakness—An Unusual Presentation of Celiac Disease. Department of Pediatrics, Postgraduate Institute of Medical Education and Research PGIMER), Chandigarh, India </sup></p>
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<p>53. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Alawneh%20K%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Alawneh K</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Ashley%20C%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Ashley C</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Carlson%20JA%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Carlson JA</b></a>. Neutrophilic myositis as a manifestation of celiac disease: a case report. Journal of Tropical Pediatrics 2002 48(6):380-381; doi:10.1093/tropej/48.6.380. © 2002 by <a href="http://tropej.oxfordjournals.org/misc/terms.dtl">Oxford University Press</a> <a href="http://www.ncbi.nlm.nih.gov/pubmed/18180977">http://www.ncbi.nlm.nih.gov/pubmed/18180977</a></p>
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<p>54. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Hardoff%20D%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Hardoff D</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Sharf%20B%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Sharf B</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Berger%20A%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Berger A</b></a>. Myopathy as a presentation of coeliac disease. <a href="http://www.ncbi.nlm.nih.gov/">Dev Med Child Neurol.</a> 1980 Dec;22(6):781-3.</p>
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<p>55. <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Goel%20NK%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Goel NK</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22McBane%20RD%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">McBane RD</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Kamath%20PS%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Kamath PS</a>. Cardiomyopathy associated with celiac disease. <a href="http://www.ncbi.nlm.nih.gov/">Mayo Clin Proc.</a> 2005 May;80(5):674-6. <a href="http://www.ncbi.nlm.nih.gov/pubmed/15887437">http://www.ncbi.nlm.nih.gov/pubmed/15887437</a></p>
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<dt>
<p>56. Nidhi Narula<sup>a</sup>, Pawan Rawal<sup>b</sup>, Rohit Manoj Kumar<sup>a</sup> and Babu Ram Thapa<sup>b</sup>&#160; Association of Celiac Disease with Cardiomyopathy and Pulmonary Hemosiderosis. Oxford Journals. Journal of Tropical Pediatrics Advance Access published online on November 6, 2009. Journal of Tropical Pediatrics, doi:10.1093/tropej/fmp088. <a href="http://tropej.oxfordjournals.org/cgi/content/abstract/fmp088v1">http://tropej.oxfordjournals.org/cgi/content/abstract/fmp088v1</a></p>
</p>
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<p>57. Mario Curione, Maria Barbato, Pietro Cugini, Silvia Amato, Silvia Da Ros, Simonetta Di Bona.&#160; Association of cardiomyopathy and celiac disease: an almost diffuse but still less know entity. Arch Med Sci 2008; 4, 2: 103–107. <a href="http://www.termedia.pl/magazine.php?magazine_id=19&amp;article_id=10658&amp;magazine_subpage=ABSTRACT">http://www.termedia.pl/magazine.php?magazine_id=19&amp;article_id=10658&amp;magazine_subpage=ABSTRACT</a></p>
</p>
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<p>58. Lodha, Ankur MD; Haran, Mehandi MD; Hollander, Gerald MD; Frankel, Robert MD; Shani, Jacob MD. Celiac Disease Associated with Dilated Cardiomyopathy. Southern Medical Journal: October 2009 – Volume 102 – Issue 10 – pp 1052-1054. </p>
<p>59. Tarcisio Not<sup>a</sup>, Elena Faleschini<sup>a</sup>, Alberto Tommasini<sup>a</sup>, Alessandra Repetto<sup>b</sup>, Michele Pasotti<sup>b</sup>, Valentina Baldas<sup>a</sup>, Andrea Spano<sup>a</sup>, Daniele Sblattero<sup>c</sup>, Roberto Marzari<sup>c</sup>, Carlo Campana<sup>b</sup>, Antonello Gavazzi<sup>d</sup>, Luigi Tavazzi<sup>b</sup>, Federico Biagi<sup>e</sup>, Gino Roberto Corazza<sup>e</sup>, Alessandro Ventura<sup>a</sup> and Eloisa Arbustini<sup>f</sup><sup>,*</sup> Celiac disease in patients with sporadic and inherited cardiomyopathies and in their relatives.<strong> </strong>European Heart Journal 2003 24(15):1455-1461; doi:10.1016/S0195-668X(03)00310-5. <a href="http://eurheartj.oxfordjournals.org/cgi/content/abstract/24/15/1455">http://eurheartj.oxfordjournals.org/cgi/content/abstract/24/15/1455</a></p>
</p>
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<dt>
<p>60. M. Curione<a name="m4.bcor*"></a><a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4B2H63Y-2C&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106295911&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=04cd9d0bb573623019a0c58817041a10#m4.cor*"><sup><img title="Corresponding Author Contact Information" border="0" alt="Corresponding Author Contact Information" src="http://www.sciencedirect.com/scidirimg/entities/REcor.gif" /></sup></a><sup>, </sup><a href="mailto:mario.curione@uniroma.it."><sup><img title="E-mail The Corresponding Author" border="0" alt="E-mail The Corresponding Author" src="http://www.sciencedirect.com/scidirimg/entities/REemail.gif" /></sup></a>, M. Barbato<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4B2H63Y-2C&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106295911&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=04cd9d0bb573623019a0c58817041a10#aff2"><sup>b</sup></a>, F. Viola2<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4B2H63Y-2C&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106295911&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=04cd9d0bb573623019a0c58817041a10#aff2"><sup>b</sup></a>, P. Francia<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4B2H63Y-2C&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106295911&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=04cd9d0bb573623019a0c58817041a10#aff1"><sup>a</sup></a>, L. De Biase<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4B2H63Y-2C&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106295911&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=04cd9d0bb573623019a0c58817041a10#aff3"><sup>c</sup></a> and S. Cucchiara<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4B2H63Y-2C&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106295911&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=04cd9d0bb573623019a0c58817041a10#aff2"><sup>b</sup></a>&#160; Idiopathic dilated cardiomyopathy associated with coeliac disease: the effect of a gluten-free diet on cardiac performance. <a href="http://www.sciencedirect.com/science/journal/15908658"><b>Digestive and Liver Disease</b></a> <a href="http://www.sciencedirect.com/science?_ob=PublicationURL&amp;_tockey=%23TOC%2312914%232002%23999659987%23471463%23FLP%23&amp;_cdi=12914&amp;_pubType=J&amp;view=c&amp;_auth=y&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=6e8b6a75e843b0ba4c415a8cbc30090f">Volume 34, Issue 12</a>, December 2002, Pages 866-869. <b><a href="http://tinyurl.com/y9hhwjt">http://tinyurl.com/y9hhwjt</a></b></p>
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<p>61. <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Jorge%20O%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Jorge O</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Jorge%20A%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Jorge A</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Camus%20G%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Camus G</a>. Celiac disease associated with antiphospholipid syndrome. <a href="http://www.ncbi.nlm.nih.gov/">Rev Esp Enferm Dig.</a> 2008 Feb;100(2):102-3.</p>
</p>
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<p>62. R Shamir, Y Shoenfeld, M Blank, R Eliakim, N Lahat, E Sobel, E Shinar, A Lerner. The prevalence of coeliac disease antibodies in patients with the antiphospholipid syndrome. Division of Paediatric Gastroenterology and Nutrition, Meyer Children’s Hospital of Haifa, Haifa, Israel, <a href="mailto:shamirr@netvision.net.il">shamirr@netvision.net.il</a>. Department of Paediatrics, Carmel Medical Center, Bruce Rappaport School of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.</p>
</p>
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<p>63. P.Rush, R.Inman, M.Bernstein, P.Carlen, L.Resch. Isolated vasculitis of the central nervous system in a patient with celiac disease. <em>The American Journal of Medicine</em>, Volume 81, Issue 6, Pages 1092-1094 </p>
</p>
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<p>64. S Meyers, S Dikman, H Spiera, N Schultz, H D Janowitz. Cutaneous vasculitis complicating coeliac disease. <i>Gut</i> 1981;<b>22</b>:61-64; doi:10.1136/gut.22.1.61 </p>
</p>
</dt>
<dt>
<p>65. V. Alegre, R. Winkelmann, J. Diez-Martin, P. Banks. Adult celiac disease, small and medium vessel cutaneous necrotizing vasculitis, and T cell lymphoma† <em>Journal of the American Academy of Dermatology</em>, Volume 19, Issue 5, Pages 973-978.</p>
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<dt>
<p>67. Ola Olén<img alt="" src="http://informahealthcare.com/entityImage/?code=200B" />?<sup>1</sup>,<sup>2</sup><sup>†</sup>, Scott M. Montgomery<img alt="" src="http://informahealthcare.com/entityImage/?code=200B" />?<sup>3</sup>,<sup>4</sup><sup>5</sup>, Göran Elinder<img alt="" src="http://informahealthcare.com/entityImage/?code=200B" />?<sup>1</sup>,<sup>2</sup>, Anders Ekbom<img alt="" src="http://informahealthcare.com/entityImage/?code=200B" />?<sup>3</sup>,<sup>6</sup> and Jonas F. Ludvigsson<img alt="" src="http://informahealthcare.com/entityImage/?code=200B" />?<sup>3</sup>,<sup>7</sup> Increased risk of immune thrombocytopenic purpura among inpatients with coeliac disease. <a href="http://informahealthcare.com/loi/gas">Scandinavian Journal of Gastroenterology</a> 2008, Vol. 43, No. 4, Pages 416-422. </p>
<p>68. L. STENHAMMAR <sup>1</sup> <a href="http://www3.interscience.wiley.com/journal/120015953/abstract#c1"></a><a href="http://www3.interscience.wiley.com/journal/120015953/abstract#c1">C. G. LJUNGGREN <sup>1</sup>&#160;</a> Thrombocytopenic Purpura and Coeliac Disease. <a href="http://www3.interscience.wiley.com/journal/117988202/home">Acta Pædiatrica</a>&#160;<strong><a href="http://www3.interscience.wiley.com/journal/120015923/issue">Volume 77 Issue 5</a>, Pages 764 – 766</strong></p>
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<p>69. Alessio Fasano, M.D. Physiological, Pathological, and Therapeutic Implications of Zonulin-Mediated Intestinal Barrier Modulation. American Journal of Pathology, 2008;173:1243-1252.</p>
</dt>
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<p>70. Rensch M.J. et el. The Prevalence Of Celiac Disease Autoantibodies In Patients With Systemic Lupus Erythematosus. American Journal Of Gastroenterology 96 (2001):1113-5. In this study, the researchers found antigliadin antibodies in some individuals with Lupus. The IgA antiendomysial antibodies and scopes were negative, so the researchers thought the antigliadin results were false negatives. IgA antiendomysial antibodies correspond with the level of intestinal damage so this test would likely be negative considering that the scope results were negative (also could have a IgA deficiency). Many with CD do not have bowel involvement, so I think the positive antigliadin antibodies in this study could indicate that these people are gluten sensitive (similar to gluten ataxia).</p>
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<p>71. Hadjivassilou et el. Gluten Sensitivity Masquerading As Systemic&#160; Lupus Erythematosus. Annals Of Rheumatic Diseases 63 (2004): 1501-3.</p>
</dt>
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<p>72. Peter Elfström<sup>*</sup>, Scott M. Montgomery, Olle Kämpe, Anders Ekbom, and Jonas F. Ludvigsson. Risk of primary adrenal insufficiency in patients with celiac disease. Journal of Clinical Endocrinology &amp; Metabolism doi:10.1210/jc.2007-0960.</p>
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		<title>Part 10 Of 12 Part Series: Heart and Lung Symptoms In Undiagnosed Celiac Disease</title>
		<link>http://celiacnurse.com/heart-and-lung-symptoms-in-undiagnosed-celiac-disease-or-with-gluten-sensitivity/</link>
		<comments>http://celiacnurse.com/heart-and-lung-symptoms-in-undiagnosed-celiac-disease-or-with-gluten-sensitivity/#comments</comments>
		<pubDate>Fri, 27 Nov 2009 21:26:54 +0000</pubDate>
		<dc:creator>Shelly</dc:creator>
				<category><![CDATA[12 Part Series: CD Symptoms]]></category>

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		<description><![CDATA[This is the tenth in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, heart and lung symptoms will be discussed. There are studies, articles, and books identifying an association between CD, cardiac (heart), and pulmonary (lung) symptoms. The pathogenesis is likely due [...]]]></description>
			<content:encoded><![CDATA[<p>This is the tenth in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, heart and lung symptoms will be discussed. There are studies, articles, and books identifying an association between CD, cardiac (heart), and pulmonary (lung) symptoms. The pathogenesis is likely due to autoimmune reactions (to ingested gluten), causing inflammation and damage to the cardiopulmonary system, in genetically predisposed individuals (1-39,44,45,61).</p>
<p><span id="more-303"></span></p>
<h3>Cardiac (Heart) Symptoms</h3>
<p>A functional cardiac system is dependent on intact blood vessels, adequate blood supply, intact cardiac nervous system and functional cardiac muscle. Hypothetically, cardiac symptoms may result from auto-antibodies (to ingested gluten) cross-reacting with blood vessels (might inhibit angiogenesis), the cardiac nervous system, or the cardiac muscle. Since we know immune reactions to gluten can affect the nervous system (ex. gluten ataxia or neuropathies) and the muscular system (ex. myopathies), it is reasonable to suspect that these two systems, involved in cardiac health, could be affected. The finding of anti-transglutaminase antibodies in end-stage heart failure and cardiomyopathy increases this possibility. With blood vessels, one study demonstrated angiogenesis was inhibited in the intestine of CD patients and the researchers suspect that impaired angiogenesis could occur in other areas of the body as well. Auto-antibodies have been found around blood vessels in the brain of CD patients, it is plausible to suspect that autoimmune reactions against tissue transglutaminase could occur around the vessels of the heart as well.&#160; Associated vasculitis, leading to stenosis, occlusions, or aneurysm of the blood vessels, may add to impaired  cardiovascular health in CD (1,7-10,12,13,15-22,44,45,54,57-59,61). </p>
<p>In some individuals with CD, the intestinal villi responsible for absorbing nutrients becomes damaged, creating a flattened mucosal surface (villous flattening). Autoimmune reactions to ingested gluten cross-react with intestinal villi and create this damage. Various nutrient deficiencies can occur and this can cause or add to the severity of the cardiac and pulmonary symptoms (1-3,40-43).&#160; <strong>Nutrient deficiencies</strong> that may affect the cardiac nervous system, cardiac muscle, and the functional structure of the heart and lungs include <strong>vitamins A, D, E, K, B complex, amino and fatty acids, calcium, magnesium, phosphorus, copper, electrolytes, iodine, iron, zinc, manganese, selenium, l-carnitine, antioxidants, and inositrol. </strong>Examples demonstrating a cardiac impact include thiamine deficiency leading to wet beriberi or acute pernicious beriberi, low electrolytes (or magnesium, calcium) leading to arrhythmias, low iron and B vitamins leading to anemia, or low vitamin K levels affecting protein S or protein C (involved in clotting) possibly leading to a heart attack. The presence of associated antiphospholipid syndrome could increase the risk of clots as well. Hypotension (a cardiac stressor) could result from low protein levels (ex. albumin), low electrolytes, or dehydration especially if diarrhea and vomiting is present. As well, other deficiencies could affect the cardiac structure or nervous system leading to many possible cardiac symptoms (7,11-14,15,42,43,51-53,55,56,59,93,99). </p>
<p>In studies (including case studies), books, and articles, cardiac conditions associated with CD include idiopathic dilated cardiomyopathy (fairly well known association), heart failure, angina, myocardial infarction (heart attack), cardiomegally, pericarditis, myocarditis, arrhythmias, and atrioventricular heart block. ECG and tissue doppler imaging results were mentioned in 2 studies. ECG changes showed prolonged QT-period with ventricular bigeminus in an adult. Doppler imaging of the heart revealed myocardial systolic wave velocity (of the mitral annulus) was low and the left ventricle had subclinical systolic dysfunction (in children) (1,7-10,12,13,15-22,44,45,61). Further research is needed to examine the possible role of CD in other heart conditions.</p>
<p>The good news is that a strict gluten-free diet should effectively eliminate the auto-antibodies leading to better cardiac health in most individuals. There is always a risk though of irreversible permanent damage (7,9,11,12,19,20,22,33,47-49,50-59). </p>
<p><em>24 years ago, I was diagnosed with mitral valve prolapse. I experienced palpitations which lead to the diagnosis. Approximately, 20 years later, doppler imaging demonstrated that I no longer had this heart condition. Was it misdiagnosed (diagnostic tests are more accurate now) or did a gluten free diet somehow help to correct it?.</em><br />
<h3><strong>Pulmonary (Lung) Symptoms</strong></h3>
<p>A functional pulmonary system is reliant on the structural integrity of the lungs, the autonomic nervous system, a healthy heart, and a healthy vascular supply of blood. Hypothetically, pulmonary symptoms may result from auto-antibodies directed at blood vessels (might inhibit angiogenesis), the autonomic nervous system, the cardiac system (as discussed above), or the lung tissue. As mentioned under cardiac symptoms, we know that auto-antibodies can affect nerves, muscle, and vascular tissue, it is reasonable to suspect that the smooth muscle and other lungs tissue along with the autonomic nervous system may be affected in CD (47-50,54).&#160; </p>
<p>There are other factors that may affect pulmonary function. The presence of vasculitis (also could cause Wegener&#8217;s Granulomatosis), antiphospholipid syndrome, along with protein S and C abnormalities could increase the risk for clots (pulmonary embolus). Conversely, low vitamin K levels, due to malabsorption could lead to diffuse pulmonary bleeding. As well, the presence of anemia (common in CD) may impair the supply of oxygen to the cells causing further distress. If heart failure occurs, pulmonary edema (fluid in the lungs) could also impair oxygen exchange. An additional concern is that chronic tissue damage might increase the risk of lung cancer. Collectively or individually, these factors along with nutrient deficiencies (such as vitamin A deficiency leading to loss of cilia and and mucin in lungs) could lead to a variety of pulmonary symptoms (33,51-59,68).</p>
<p>In studies (including case studies) and articles, pulmonary conditions may include lung infections, lung abscesses, increased susceptibility to tuberculosis, bronchiectasis, pneumonia, pulmonary hemosiderosis, fibrosing alveolitis of the lung, and possibly pneumococcal septicemia. There were a few case studies mentioning an association between cystic fibrosis and CD as well. In one study, cystic fibrosis patients had a higher prevalence of CD than in the general population. The researchers recommended that individuals with cystic fibrosis should be screened for CD (if they live in a population where CD exists). There is evidence that tissue transglutaminase is elevated in cystic fibrosis. Perhaps auto-antibodies (ex. anti-tissue transglutaminase) react to this overproduction and cross-react with the lungs, similar to the response seen in the bowel, brain, and heart of individuals with CD/gluten sensitivities (2-8,14,23-31,45,49,50,60,61). </p>
<p>Further research is needed to examine the cystic fibrosis/CD connection, and possible autoimmune effects&#160; with other lung diseases, such as asthma. My mother, daughter, and I all have CD and asthma. I have talked to many others with CD and asthma as well. Could gluten sensitivity be responsible for many other lung diseases as well? More research is needed. </p>
<h3><strong>Other Contributing Factors</strong></h3>
<p>Other factors that may contribute to cardiopulmonary symptoms include smoking, hypertension, diabetes, hyperlipidemia, hyperhomocysteinemia (associated with CD), renal failure, bleeding (hemorrhage), thyroid disease, trauma, infections, genetics, toxic-metabolic agents, certain medications, poor diet, vitamin deficiency or toxicity, alcoholism, heavy metals, solvents, street drugs, and past gastric or intestinal surgery (leading to deficiencies) (14,15,42,43,46).</p>
<h3><strong>Diagnosis</strong></h3>
<p>There are a number of tests to consider when diagnosing gluten sensitivities. <strong>IgA endomysial antibodies and anti-transglutaminase antibodies are useful blood tests along with an upper endoscopy</strong> <strong>with multiple biopsies</strong> (to investigate intestinal involvement) (1,5,6,152). Antibodies against deamidated gluten should be added to the screening process as well (69). If the patient has <strong>IgA deficiency then IgG tissue transglutaminase</strong> <strong>antibody test</strong> may be helpful. As well, <strong>IgG and IgA antigliadin antibodies</strong> may be helpful to identify if increased intestinal permeability has allowed gluten (gliadin) to leak in through the tight junctions between the intestinal epithelial cells. This leakage could potentially lead to a gluten sensitivity and with continued exposure potentially CD. Positive IgG and IgA antigliadin antibodies can indicate that a gluten sensitivity exists (1,5,6,45,62-64). </p>
<p>Additional tests are available as well, such as HLA genetic testing, fecal tests, and rectal mucosal patch technique (new in Sweden) (1,62,63,115,146). It is important to explore the presence of nutrient deficiencies as well.</p>
<h3><strong>Do You Have Any Of The Above Symptoms?</strong></h3>
<p>CD can be present in children that are growing normally so normal growth rate should not be a factor that excludes the possibility of CD (65). Many individuals with undiagnosed CD/gluten sensitivities will have no bowel symptoms. Weight loss may or may not occur, and is dependent on the amount of the intestine that is damaged (1-3). Therefore, the symptoms in this post could occur in the absence of stunted growth, weight loss, or bowel symptoms.</p>
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<p>The presence of cardiopulmonary symptoms as discussed in this post, indicates that you should <strong>talk to your MD about</strong> <strong>tests for gluten sensitivities/CD and tests to rule out other possible causes of your symptoms.</strong> Testing for CD/gluten sensitivities is important because undiagnosed CD increases the risk of developing other autoimmune diseases, lymphomas (skin, brain, lymph nodes, intestine), cancers (thyroid, esophageal, mouth, tongue, pharynx, tonsil, and small intestine), allergies, complications from malabsorption issues, possible decreased immune response to other illnesses (1,2,62,63,67), and many other health complications that will be discussed in the posts about CD/gluten sensitivity symptoms. It is my hope that if you have cardiopulmonary symptoms you can print out this post complete with medical references to take with you to the MD when you request testing. Highlight or underline the sections that apply to your symptoms. I’ll be posting a simplified summary and checklist in the 12th post.</p>
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<p>It is possible to have a gluten sensitivity even if you test negative for CD. It is also possible that some of your symptoms could be due to a food allergy/sensitivity or other disease process. Allergy testing, and/or an elimination diet may help you to identify offending foods. Other tests can help rule out other diseases. I encourage everyone to have their symptoms thoroughly investigated by their MD and specialists before implementing a therapeutic diet. A consultation with a Registered Dietitian can provide guidance to ensure all nutritional needs are met. Keep your MD informed about any dietary changes you are making and also the results. Of course, I would love to hear your story as well.</p>
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<p><strong>I </strong><strong>recommend waiting until CD/gluten sensitivity testing is complete before initiating a gluten-free diet because it may create a false negative. Discuss this with your MD or specialist. <strong>USE CAUTION WITH SUPPLEMENTS. </strong>Toxicities can occur with over supplementation and this can lead to permanent damage. Consult your MD, Registered Dietitian, or other medical specialists involved in your care to determine which nutrients should be supplemented and to identify appropriate dosages for you.</strong> <strong>Review your symptoms and everything in this post with a Medical Doctor</strong> <strong>and your specialists before you make any changes</strong>. <strong>Your MD knows your medical history and the treatments that are appropriate for you.</strong></p>
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<p><strong>D</strong><strong>iagnosed Celiacs and people with food allergies/sensitivities</strong>, please comment about your symptoms&#160; and experiences at the end of each post. This will help other readers to see how the sometimes illusive symptoms of CD or food sensitivities can affect each of us.&#160; We are all unique!</p>
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<h3><strong>References</strong></h3>
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<h3><strong></strong></h3>
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<p>1. <cite><strong>Excellent Book:</strong> Green PHR, Jones, R. Celiac Disease A Hidden Epidemic. Collins, Harper Collins Publishers, 2006 <b>http://tinyurl.com/ljeqjc</b></cite></p>
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<p><cite></cite><cite>2. </cite>Pruessner Harold T, MD. Detecting Celiac Disease In Your Patients. American Family Physician. March 1st, 1998.</p>
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<p>3. Feldman Mark, MD, Friedman Lawrence S, MD, Sleisenger, Marvin H, MD, Gastrointestinal and Liver Disease Pathophysiology/Diagnosis/Management 7th Edition, Volume11, 2002,Saunders</p>
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<p>4. F.M. Stevens, C.E. Connolly, J.P. Murray, C.F. McCarthy. Lung Cavities in Patients with Coeliac Disease.&#160; <i>Digestion</i> 1990;46:72-80 </p>
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<p>5. <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Williams%20AJ%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Williams AJ</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Asquith%20P%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Asquith P</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Stableforth%20DE%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Stableforth DE</a>. Susceptibility to tuberculosis in patients with coeliac disease. <a href="http://www.ncbi.nlm.nih.gov/">Tubercle.</a> 1988 Dec;69(4):267-74.</p>
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<p>6. J F Ludvigsson<sup>1</sup><sup>,2</sup>, J Wahlstrom<sup>3</sup>, J Grunewald<sup>3</sup>, A Ekbom<sup>2</sup><sup>,4</sup>, S M Montgomery<sup>2</sup><sup>,5</sup>&#160;&#160; Coeliac disease and risk of tuberculosis: a population based cohort study. Published Online First: 17 October 2006. doi:10.1136/thx.2006.059451       <br /><i>Thorax</i> 2007;<b>62</b>:23-28 </p>
<h5>7. <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Goel%20NK%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Goel NK</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22McBane%20RD%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">McBane RD</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Kamath%20PS%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Kamath PS</a>. Cardiomyopathy associated with celiac disease. <a href="http://www.ncbi.nlm.nih.gov/">Mayo Clin Proc.</a> 2005 May;80(5):674-6. <a title="http://www.ncbi.nlm.nih.gov/pubmed/15887437" href="http://www.ncbi.nlm.nih.gov/pubmed/15887437">http://www.ncbi.nlm.nih.gov/pubmed/15887437</a>&#160;</h5>
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<p>8. Nidhi Narula<sup>a</sup>, Pawan Rawal<sup>b</sup>, Rohit Manoj Kumar<sup>a</sup> and Babu Ram Thapa<sup>b</sup>&#160; Association of Celiac Disease with Cardiomyopathy and Pulmonary Hemosiderosis. Oxford Journals. Journal of Tropical Pediatrics Advance Access published online on November 6, 2009. Journal of Tropical Pediatrics, doi:10.1093/tropej/fmp088. <a title="http://tropej.oxfordjournals.org/cgi/content/abstract/fmp088v1" href="http://tropej.oxfordjournals.org/cgi/content/abstract/fmp088v1">http://tropej.oxfordjournals.org/cgi/content/abstract/fmp088v1</a>&#160;</p>
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<p>9. Mario Curione, Maria Barbato, Pietro Cugini, Silvia Amato, Silvia Da Ros, Simonetta Di Bona.&#160; Association of cardiomyopathy and celiac disease: an almost diffuse but still less know entity. Arch Med Sci 2008; 4, 2: 103–107. <a title="http://www.termedia.pl/magazine.php?magazine_id=19&amp;article_id=10658&amp;magazine_subpage=ABSTRACT" href="http://www.termedia.pl/magazine.php?magazine_id=19&amp;article_id=10658&amp;magazine_subpage=ABSTRACT">http://www.termedia.pl/magazine.php?magazine_id=19&amp;article_id=10658&amp;magazine_subpage=ABSTRACT</a></p>
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<p>10. Lodha, Ankur MD; Haran, Mehandi MD; Hollander, Gerald MD; Frankel, Robert MD; Shani, Jacob MD. Celiac Disease Associated with Dilated Cardiomyopathy. Southern Medical Journal: October 2009 &#8211; Volume 102 &#8211; Issue 10 &#8211; pp 1052-1054. </p>
<p>11. Tarcisio Not<sup>a</sup>, Elena Faleschini<sup>a</sup>, Alberto Tommasini<sup>a</sup>, Alessandra Repetto<sup>b</sup>, Michele Pasotti<sup>b</sup>, Valentina Baldas<sup>a</sup>, Andrea Spano<sup>a</sup>, Daniele Sblattero<sup>c</sup>, Roberto Marzari<sup>c</sup>, Carlo Campana<sup>b</sup>, Antonello Gavazzi<sup>d</sup>, Luigi Tavazzi<sup>b</sup>, Federico Biagi<sup>e</sup>, Gino Roberto Corazza<sup>e</sup>, Alessandro Ventura<sup>a</sup> and Eloisa Arbustini<sup>f</sup><sup>,*</sup> Celiac disease in patients with sporadic and inherited cardiomyopathies and in their relatives.<strong> </strong>European Heart Journal 2003 24(15):1455-1461; doi:10.1016/S0195-668X(03)00310-5. <a title="http://eurheartj.oxfordjournals.org/cgi/content/abstract/24/15/1455" href="http://eurheartj.oxfordjournals.org/cgi/content/abstract/24/15/1455">http://eurheartj.oxfordjournals.org/cgi/content/abstract/24/15/1455</a></p>
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<p>12. M. Curione<a name="m4.bcor*"></a><a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4B2H63Y-2C&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106295911&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=04cd9d0bb573623019a0c58817041a10#m4.cor*"><sup><img title="Corresponding Author Contact Information" border="0" alt="Corresponding Author Contact Information" src="http://www.sciencedirect.com/scidirimg/entities/REcor.gif" /></sup></a><sup>, </sup><a href="mailto:mario.curione@uniroma.it."><sup><img title="E-mail The Corresponding Author" border="0" alt="E-mail The Corresponding Author" src="http://www.sciencedirect.com/scidirimg/entities/REemail.gif" /></sup></a>, M. Barbato<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4B2H63Y-2C&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106295911&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=04cd9d0bb573623019a0c58817041a10#aff2"><sup>b</sup></a>, F. Viola2<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4B2H63Y-2C&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106295911&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=04cd9d0bb573623019a0c58817041a10#aff2"><sup>b</sup></a>, P. Francia<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4B2H63Y-2C&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106295911&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=04cd9d0bb573623019a0c58817041a10#aff1"><sup>a</sup></a>, L. De Biase<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4B2H63Y-2C&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106295911&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=04cd9d0bb573623019a0c58817041a10#aff3"><sup>c</sup></a> and S. Cucchiara<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4B2H63Y-2C&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106295911&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=04cd9d0bb573623019a0c58817041a10#aff2"><sup>b</sup></a>&#160; Idiopathic dilated cardiomyopathy associated with coeliac disease: the effect of a gluten-free diet on cardiac performance. <a href="http://www.sciencedirect.com/science/journal/15908658"><b>Digestive and Liver Disease</b></a>&#160;<a href="http://www.sciencedirect.com/science?_ob=PublicationURL&amp;_tockey=%23TOC%2312914%232002%23999659987%23471463%23FLP%23&amp;_cdi=12914&amp;_pubType=J&amp;view=c&amp;_auth=y&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=6e8b6a75e843b0ba4c415a8cbc30090f">Volume 34, Issue 12</a>, December 2002, Pages 866-869. <b><a href="http://tinyurl.com/y9hhwjt">http://tinyurl.com/y9hhwjt</a></b> </p>
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<p>13. Ricardo Schmit T De Bem<sup>1, 4 <a href="http://www.springerlink.com/content/t13467701v3648nu/#ContactOfAuthor1"><img border="0" alt="Contact Information" src="http://www.springerlink.com/images/contact.gif" /></a></sup>, Shirley Ramos Da Ro Sa Utiyama<sup>2</sup>, Renato Mitsunori Nisihara<sup>2</sup>, Jerônimo Antônio fortunato<sup>3</sup>, josuÉ Augusto Tondo<sup>3</sup>, Eliane Ribeiro Carmes<sup>1</sup>, Raquel Almada E. Souza<sup>1</sup>, Julio CÉsar Pisani<sup>1</sup> and Heda Maria Barska Dos Santos Amarante<sup>1</sup> Celiac Disease Prevalence in Brazilian Dilated Cardiomyopathy Patients. Journal <a href="http://www.springerlink.com/content/101150/?p=5c982f6b7800465dba51ad9a86e3c960&amp;pi=0">Digestive Diseases and Sciences</a> Issue <a href="http://www.springerlink.com/content/p402771um4v3/?p=5c982f6b7800465dba51ad9a86e3c960&amp;pi=0">Volume 51, Number 5 / May, 2006</a>&#160; <a title="http://www.springerlink.com/content/t13467701v3648nu/" href="http://www.springerlink.com/content/t13467701v3648nu/">http://www.springerlink.com/content/t13467701v3648nu/</a></p>
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<p>14. Ravi Mahadeva,<sup>a</sup> Christopher Flower,<sup>b</sup> John Shneerson<sup>a</sup>&#160; Bronchiectasis in association with coeliac disease. <i>Thorax</i> 1998;<b>53</b>:527-529; doi:10.1136/thx.53.6.527 </p>
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<p>15. Tugcin B. Polat<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4RGFYFB-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106390245&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=3584b115b39f0c820c404bea636a5af8#aff1"><sup>a</sup></a><sup>,</sup>, Nafiye Urganci<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4RGFYFB-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106390245&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=3584b115b39f0c820c404bea636a5af8#aff2"><sup>b</sup></a>, Yalim Yalcin<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4RGFYFB-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106390245&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=3584b115b39f0c820c404bea636a5af8#aff1"><sup>a</sup></a>, Cenap Zeybek<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4RGFYFB-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106390245&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=3584b115b39f0c820c404bea636a5af8#aff1"><sup>a</sup></a>, Celal Akdeniz<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4RGFYFB-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106390245&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=3584b115b39f0c820c404bea636a5af8#aff1"><sup>a</sup></a>, Abdullah Erdem<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4RGFYFB-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106390245&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=3584b115b39f0c820c404bea636a5af8#aff1"><sup>a</sup></a>, Elnur Imanov<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4RGFYFB-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106390245&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=3584b115b39f0c820c404bea636a5af8#aff1"><sup>a</sup></a> and Ahmet Celebi<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7582-4RGFYFB-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1106390245&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=3584b115b39f0c820c404bea636a5af8#aff1"><sup>a</sup></a>&#160; Cardiac functions in children with coeliac disease during follow-up: Insights from tissue Doppler imaging. <a href="http://www.sciencedirect.com/science/journal/15908658"><b>Digestive and Liver Disease</b></a>&#160;<a href="http://www.sciencedirect.com/science?_ob=PublicationURL&amp;_tockey=%23TOC%2312914%232008%23999599996%23679868%23FLA%23&amp;_cdi=12914&amp;_pubType=J&amp;view=c&amp;_auth=y&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=e6b3a9bb99fefec13259a7fde7cdd632">Volume 40, Issue 3</a>, March 2008, Pages 182-187. <b><a href="http://tinyurl.com/ydzutq7">http://tinyurl.com/ydzutq7</a></b> </p>
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<p>16. <em>WEI, L. *; SPIERS, E. +; REYNOLDS, N. ++; WALSH, S. [S]; FAHEY, T. [P]; MACDONALD, T. M. *</em>&#160;&#160; The association between coeliac disease and cardiovascular disease. Alimentary Pharmacology &amp; Therapeutics. 27(6):514-519, March 15, 2008. <b><a href="http://tinyurl.com/yeyw2aw">http://tinyurl.com/yeyw2aw</a></b> </p>
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<p>17. <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Siry%20M%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Siry M</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Burges%20C%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Burges C</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Stiens%20R%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Stiens R</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Schneider%20H%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Schneider H</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Steiff%20J%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Steiff J</a>. [First diagnosis of celiac disease in a 67-year old female patient]. <a href="http://www.ncbi.nlm.nih.gov/">Dtsch Med Wochenschr.</a> 2000 Aug 4;125(31-32):932-6.</p>
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<p>18. Loren A. Laine, MD; Kenneth M. Holt, MD. Recurrent Pericarditis and Celiac Disease. <em>JAMA.</em> 1984;252(22):3168.</p>
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<p><cite>44. </cite>Vincent Cottin<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7J28-4KPNHVN-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1109906306&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=8f46ebfd50348936c67855e4b9548c2e#aff1"><sup>a</sup></a><sup>,</sup>, Gael Clérici<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7J28-4KPNHVN-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1109906306&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=8f46ebfd50348936c67855e4b9548c2e#aff2"><sup>b</sup></a>, Nicole Fabien<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7J28-4KPNHVN-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1109906306&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=8f46ebfd50348936c67855e4b9548c2e#aff3"><sup>c</sup></a>, Hugues Rousset<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7J28-4KPNHVN-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1109906306&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=8f46ebfd50348936c67855e4b9548c2e#aff4"><sup>d</sup></a> and Jean-François Cordier<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7J28-4KPNHVN-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1109906306&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=8f46ebfd50348936c67855e4b9548c2e#aff1"><sup>a</sup></a>&#160; Celiac disease revealed by diffuse alveolar hemorrhage and heart block. <a href="http://www.sciencedirect.com/science/journal/17449049"><b>Respiratory Medicine Extra</b></a>&#160;<a href="http://www.sciencedirect.com/science?_ob=PublicationURL&amp;_tockey=%23TOC%2321376%232006%23999979996%23634537%23FLA%23&amp;_cdi=21376&amp;_pubType=J&amp;view=c&amp;_auth=y&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=58937cf5639dd24d80abefdd3555e403">Volume 2, Issue 3</a>, 2006, Pages 89-91.</p>
</dt>
<dt>
<p>45. Maddalena Peracchi MD<sup><a href="http://www.nature.com/ajg/journal/v97/n11/abs/ajg2002723a.html#aff1">1</a></sup>, Cristina Trovato MD<sup><a href="http://www.nature.com/ajg/journal/v97/n11/abs/ajg2002723a.html#aff1">1</a></sup>, Massimo Longhi MD<sup><a href="http://www.nature.com/ajg/journal/v97/n11/abs/ajg2002723a.html#aff2">2</a></sup>, Maurizio Gasparin DSc<sup><a href="http://www.nature.com/ajg/journal/v97/n11/abs/ajg2002723a.html#aff2">2</a></sup>, Dario Conte MD<sup><a href="http://www.nature.com/ajg/journal/v97/n11/abs/ajg2002723a.html#aff1">1</a></sup>, Cristina Tarantino BSc<sup><a href="http://www.nature.com/ajg/journal/v97/n11/abs/ajg2002723a.html#aff1">1</a></sup>, Daniele Prati MD<sup><a href="http://www.nature.com/ajg/journal/v97/n11/abs/ajg2002723a.html#aff3">3</a></sup> and Maria Teresa Bardella MD<sup><a href="http://www.nature.com/ajg/journal/v97/n11/abs/ajg2002723a.html#aff1">1</a></sup>&#160; Tissue transglutaminase antibodies in patients with end-stage heart failure. The American Journal of Gastroenterology (2002) <b>97</b>, 2850–2854; doi:10.1111/j.1572-0241.2002.07033.x.</p>
</dt>
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<p>46. <em>Alessandro Luciani<sup>*</sup><sup>,<img border="0" alt="{dagger}" src="http://www.jimmunol.org/math/dagger.gif" /></sup>, Valeria Rachela Villella<sup><img border="0" alt="{ddagger}" src="http://www.jimmunol.org/math/Dagger.gif" /></sup>, Angela Vasaturo<sup><img border="0" alt="{ddagger}" src="http://www.jimmunol.org/math/Dagger.gif" /></sup>, Ida Giardino<sup><img border="0" alt="§" src="http://www.jimmunol.org/math/sect.gif" /></sup>, Valeria Raia<sup>¶</sup>, Massimo Pettoello-Mantovani<sup>*</sup>, Maria D&#8217;Apolito<sup>*</sup>, Stefano Guido<sup><img border="0" alt="{dagger}" src="http://www.jimmunol.org/math/dagger.gif" /></sup><sup>,<img border="0" alt="{ddagger}" src="http://www.jimmunol.org/math/Dagger.gif" /></sup>, Teresinha Leal<sup>||</sup>, Sonia Quaratino<sup>#</sup> and Luigi Maiuri<a name="RFN2"></a><sup>2</sup><sup>,*</sup><sup>,**</sup></em> SUMOylation of Tissue Transglutaminase as Link between Oxidative Stress and Inflammation<a name="RFN1"></a><sup>1. </sup>Published online July 22, 2009       <br /><em>The Journal of Immunology</em>, 2009, 183, 2775 –2784.&#160; </p>
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<p>47. Wong M, et el. Proximal Myopathy And Bone Pain As The Presenting Features Of Coeliac Disease. Ann Rheum Dis, 2002, 61(1):p87-8.</p>
<p>48. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Kleopa%20KA%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus">Kleopa KA</a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Kyriacou%20K%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus">Kyriacou K</a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Zamba-Papanicolaou%20E%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus">Zamba-Papanicolaou E</a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Kyriakides%20T%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus">Kyriakides T</a>. Reversible inflammatory and vacuolar myopathy with vitamin E deficiency in celiac disease. <a href="http://www.ncbi.nlm.nih.gov/">Muscle Nerve.</a> 2005 Feb;31(2):260-5.</p>
<p>49. Albert Selva-O&#8217;Callaghan, MD, PhD<sup> 1 *</sup>, Francesc Casellas, MD, PhD<sup> 2</sup>, Ines de Torres, MD, PhD<sup> 3</sup>, Eduard Palou, MD, PhD<sup> 4</sup>, Josep M. Grau-Junyent, MD, PhD<sup> 5</sup>, Miquel Vilardell-Tarrés, MD, PhD<sup> 1 </sup><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&amp;cmd=Retrieve&amp;dopt=AbstractPlus&amp;list_uids=16967485&amp;itool=pubmed_DocSum">Celiac disease and antibodies associated with celiac disease in patients with inflammatory myopathy</a>. <a href="http://www3.interscience.wiley.com/journal/32891/home">Muscle &amp; Nerve</a>, <strong><a href="http://www3.interscience.wiley.com/journal/113518454/issue">Volume 35 Issue 1</a>, Pages 49 – 54. </strong>Published </p>
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<p>50. Hadjivassiliou M, Maki M, Saunders DS, Williamson CA, Grunewald RA, Woodroof NM, Korponay-Szabo IR. Autoantibody Targeting of Brain and Intestinal Transglutaminase in Gluten Ataxia. Neurology 2006 Feb.14;66(3):373-7.</p>
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<p>51.&#160; T Matsuzaka, H Tanaka, M Fukuda, M Aoki, Y Tsuji, and H Kondoh. Relationship between vitamin K dependent coagulation factors and anticoagulants (protein C and protein S) in neonatal vitamin K deficiency. Arch Dis Child. 1993 March; 68(3 Spec No): 297–302.</p>
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<p>52. <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Jorge%20O%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Jorge O</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Jorge%20A%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Jorge A</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Camus%20G%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Camus G</a>. Celiac disease associated with antiphospholipid syndrome. <a href="http://www.ncbi.nlm.nih.gov/">Rev Esp Enferm Dig.</a> 2008 Feb;100(2):102-3.</p>
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<p>53. Armando D’Angelo, Silvana Viganò D’Angelo. Protein S deficiency. Haematologica, Vol 93, Issue 4, 498-501 doi:10.3324/haematol.12691</p>
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<p>54. E Myrsky,<sup>*</sup> K Kaukinen,<sup>†</sup> M Syrjänen,<sup>*</sup> I R Korponay-Szabó,<sup>‡</sup> M Mäki,<sup>*</sup> and K Lindfors<sup>*&#160; Coeliac disease-specific autoantibodies targeted against transglutaminase 2 disturb angiogenesis. </sup>Clin Exp Immunol. 2008 April; 152(1): 111–119.</p>
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<p>55. Deepak Gupta<sup>1 <a href="http://www.springerlink.com/content/175866077635122g/#ContactOfAuthor1"><img border="0" alt="Contact Information" src="http://www.springerlink.com/images/contact.gif" /></a></sup> and Naureen Mirza<sup>1 <a href="http://www.springerlink.com/content/175866077635122g/#ContactOfAuthor2"><img border="0" alt="Contact Information" src="http://www.springerlink.com/images/contact.gif" /></a></sup> Systemic lupus erythematosus, celiac disease and antiphospholipid antibody syndrome: a rare association. Journal <a href="http://www.springerlink.com/content/101577/?p=49a3d64a63384df1b10774f12394396f&amp;pi=0">Rheumatology International</a>, <a href="http://www.springerlink.com/content/vjg1r2232580/?p=49a3d64a63384df1b10774f12394396f&amp;pi=0">Volume 28, Number 11 / September, 2008</a>.</p>
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<p>56. R Shamir, Y Shoenfeld, M Blank, R Eliakim, N Lahat, E Sobel, E Shinar, A Lerner. The prevalence of coeliac disease antibodies in patients with the antiphospholipid syndrome. Division of Paediatric Gastroenterology and Nutrition, Meyer Children’s Hospital of Haifa, Haifa, Israel, <a href="mailto:shamirr@netvision.net.il">shamirr@netvision.net.il</a>. Department of Paediatrics, Carmel Medical Center, Bruce Rappaport School of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.</p>
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<p>57. P.Rush, R.Inman, M.Bernstein, P.Carlen, L.Resch. Isolated vasculitis of the central nervous system in a patient with celiac disease. <em>The American Journal of Medicine</em>, Volume 81, Issue 6, Pages 1092-1094 </p>
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<p>58. S Meyers, S Dikman, H Spiera, N Schultz, H D Janowitz. Cutaneous vasculitis complicating coeliac disease. <i>Gut</i> 1981;<b>22</b>:61-64; doi:10.1136/gut.22.1.61 </p>
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<p>59. V. Alegre, R. Winkelmann, J. Diez-Martin, P. Banks. Adult celiac disease, small and medium vessel cutaneous necrotizing vasculitis, and T cell lymphoma† <em>Journal of the American Academy of Dermatology</em>, Volume 19, Issue 5, Pages 973-978.</p>
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<p>60. Siiri E. Iismaa<sup></sup>, Bryony M. Mearns<sup></sup>, Laszlo Lorand<sup></sup> and Robert M. Graham. Transglutaminases and Disease: Lessons From Genetically Engineered Mouse Models and Inherited Disorders. Physiol. Rev. 89: 991-1023, 2009. </p>
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<p>61. <em>Luigi Maiuri<a name="RFN2"></a><sup>2</sup><sup>,*</sup><sup>,<img border="0" alt="{dagger}" src="http://www.jimmunol.org/math/dagger.gif" /></sup>, Alessandro Luciani<sup><img border="0" alt="{dagger}" src="http://www.jimmunol.org/math/dagger.gif" /></sup><sup>,<img border="0" alt="{ddagger}" src="http://www.jimmunol.org/math/Dagger.gif" /></sup>, Ida Giardino<sup><img border="0" alt="§" src="http://www.jimmunol.org/math/sect.gif" /></sup>, Valeria Raia<sup>¶</sup>, Valeria R. Villella<sup>||</sup>, Maria D&#8217;Apolito<sup><img border="0" alt="{dagger}" src="http://www.jimmunol.org/math/dagger.gif" /></sup>, Massimo Pettoello-Mantovani<sup><img border="0" alt="{dagger}" src="http://www.jimmunol.org/math/dagger.gif" /></sup>, Stefano Guido<sup>||</sup>, Carolina Ciacci<sup><img border="0" alt="{ddagger}" src="http://www.jimmunol.org/math/Dagger.gif" /></sup>, Mariano Cimmino<sup>#</sup>, Olivier N. Cexus<sup>**</sup>, Marco Londei<sup><img border="0" alt="{dagger}" src="http://www.jimmunol.org/math/dagger.gif" /><img border="0" alt="{dagger}" src="http://www.jimmunol.org/math/dagger.gif" /></sup><sup>,*</sup> and Sonia Quaratino<a name="RFN2"></a><sup>2</sup><sup>,**</sup><sup>,<img border="0" alt="{dagger}" src="http://www.jimmunol.org/math/dagger.gif" /><img border="0" alt="{dagger}" src="http://www.jimmunol.org/math/dagger.gif" /></sup></em>&#160;&#160; Tissue Transglutaminase Activation Modulates Inflammation in Cystic Fibrosis via PPAR<img border="0" alt="{gamma}" src="http://www.jimmunol.org/math/large/ggr.gif" /> Down-Regulation<a name="RFN1"></a><sup>1</sup> <em>The Journal of Immunology</em>, 2008, 180, 7697 –7705.</p>
</dt>
<dt>
<p>61. Vincent Cottin<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7J28-4KPNHVN-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1112481617&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=bdf275b6e8525a4444a1dcc1d7b5f8ff#aff1"><sup>a</sup></a><sup>, </sup><a name="bcor1"></a><a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7J28-4KPNHVN-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1112481617&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=bdf275b6e8525a4444a1dcc1d7b5f8ff#cor1"><sup><img title="Corresponding Author Contact Information" border="0" alt="Corresponding Author Contact Information" src="http://www.sciencedirect.com/scidirimg/entities/REcor.gif" /></sup></a><sup>, </sup><a href="mailto:vincent.cottin@chu-lyon.fr"><sup><img title="E-mail The Corresponding Author" border="0" alt="E-mail The Corresponding Author" src="http://www.sciencedirect.com/scidirimg/entities/REemail.gif" /></sup></a>, Gael Clérici<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7J28-4KPNHVN-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1112481617&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=bdf275b6e8525a4444a1dcc1d7b5f8ff#aff2"><sup>b</sup></a>, Nicole Fabien<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7J28-4KPNHVN-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1112481617&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=bdf275b6e8525a4444a1dcc1d7b5f8ff#aff3"><sup>c</sup></a>, Hugues Rousset<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7J28-4KPNHVN-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1112481617&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=bdf275b6e8525a4444a1dcc1d7b5f8ff#aff4"><sup>d</sup></a> and Jean-François Cordier<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B7J28-4KPNHVN-1&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1112481617&amp;_rerunOrigin=google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=bdf275b6e8525a4444a1dcc1d7b5f8ff#aff1"><sup>a</sup></a>&#160; Celiac disease revealed by diffuse alveolar hemorrhage and heart block. <a href="http://www.sciencedirect.com/science/journal/17449049">Respiratory Medicine Extra</a>&#160;<a href="http://www.sciencedirect.com/science?_ob=PublicationURL&amp;_tockey=%23TOC%2321376%232006%23999979996%23634537%23FLA%23&amp;_cdi=21376&amp;_pubType=J&amp;view=c&amp;_auth=y&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=58937cf5639dd24d80abefdd3555e403">Volume 2, Issue 3</a>, 2006, Pages 89-91.</p>
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<p>62.&#160; Lieberman Shari PhD,CNC, FACN, with Linda Segall. The Gluten Connection. How Gluten Sensitivity May Be Sabotaging Your Health. Rodale Inc., 2007. </p>
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<p>63 James Braly, MD., Ron Hoggan, MA. Dangerous Grains. Penguin Group, Inc., 2002.</p>
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<p>64. Jefferson dams. Celiac G+ Antibody Assay for the Detection of Auto-antibodies in Celiac Disease. <a title="http://www.celiac.com/articles/21919/1/Celiac-G-Antibody-Assay-for-the-Detection-of-Auto-antibodies-in-Celiac-Disease/Page1.html" href="http://www.celiac.com/articles/21919/1/Celiac-G-Antibody-Assay-for-the-Detection-of-Auto-antibodies-in-Celiac-Disease/Page1.html">http://www.celiac.com/articles/21919/1/Celiac-G-Antibody-Assay-for-the-Detection-of-Auto-antibodies-in-Celiac-Disease/Page1.html</a></p>
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<p>65. Lejarraga H, et el. Normal Growth Velocity Before Diagnosis Of Celiac Disease. J Pediatr Gastrenterol Nutr 2000;30:552-556.</p>
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<p>66. Hadjivassilou M and <em>Grünwald</em> RA, Davies-Jones GAB. Gluten Sensitivity As a Neurological Illness. Journal of Neurology, Neurosurgery, and Psychiatry 2002;72:560-563 </p>
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<p>67. School of Medicine News: University of Maryland School of Medicine Scientists Pinpoint Critical Molecule to Celiac, Possibly Other Autoimmune Disorders. <em>Tuesday, September 29, 2009. <a title="http://somvweb.som.umaryland.edu/absolutenm/templates/?a=915" href="http://somvweb.som.umaryland.edu/absolutenm/templates/?a=915">http://somvweb.som.umaryland.edu/absolutenm/templates/?a=915</a>&#160;</em></p>
<p>&#160;&#160; </p>
<p>68. Diet and Human Immune Function by David A. Hughes, L. Gail Darlington, and Adrianne Bendich. Humana Press; 1 edition (Dec 4 2003)
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<p>69. S. Rashtak, M. Ettore, H. Homburger, J. Murray. Comparative Usefulness of Deamidated Gliadin Antibodies in the Diagnosis of Celiac Disease. Clinical Gastroenterology and Hepatology, Volume 6, Issue 4, Pages 426-432</p>
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		<title>Part 9 Of 12 Part Series: Psychological And Cognitive Symptoms With Undiagnosed Celiac Disease, Gluten Intolerance or Sensitivities</title>
		<link>http://celiacnurse.com/part-9-of-12-part-series-psychological-and-cognitive-symptoms-learning-disabilities-dementia-depression-mood-disorders-anxiety-and-schizophrenia-in-undiagnosed-celiac-disease/</link>
		<comments>http://celiacnurse.com/part-9-of-12-part-series-psychological-and-cognitive-symptoms-learning-disabilities-dementia-depression-mood-disorders-anxiety-and-schizophrenia-in-undiagnosed-celiac-disease/#comments</comments>
		<pubDate>Sat, 21 Nov 2009 07:41:51 +0000</pubDate>
		<dc:creator>Shelly</dc:creator>
				<category><![CDATA[12 Part Series: CD Symptoms]]></category>

		<guid isPermaLink="false">http://celiacnurse.com/part-9-of-12-part-series-psychological-and-cognitive-symptoms-learning-disabilities-dementia-depression-mood-disorders-anxiety-and-schizophrenia-in-undiagnosed-celiac-disease/</guid>
		<description><![CDATA[This is the ninth in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, psychological and cognitive symptoms will be discussed. There are studies, articles, and books identifying an association between CD/gluten sensitivities, psychological and cognitive symptoms&#160; The pathogenesis is thought to be [...]]]></description>
			<content:encoded><![CDATA[<p>This is the ninth in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, psychological and cognitive symptoms will be discussed. There are studies, articles, and books identifying an association between CD/gluten sensitivities, psychological and cognitive symptoms&#160; The pathogenesis is thought to be due to autoimmune reactions (to ingested gluten) causing inflammation and damage in the central nervous system (CNS) and the gastrointestinal tract in genetically predisposed individuals. With gastrointestinal involvement, nutrient deficiencies (common in CD), can add to the symptoms (1,5,6,10-12-14,15,19,20,23-29,32-34,37,38,41,42,55-57).<br />
<span id="more-223"></span>
</p>
<p>Many with psychological and cognitive symptoms associated with CD/gluten sensitivities do not have bowel symptoms. In others, the intestinal villi responsible for absorbing nutrients becomes damaged, creating a flattened mucosal surface (villous flattening). Autoimmune reactions to ingested gluten and related prolamines cross-react with intestinal villi and create this damage. Various nutrient deficiencies can occur and this can cause or add to the severity of the psychological and cognitive symptoms. <strong>Nutrient deficiencies</strong> contributing to psychological and cognitive symptoms can include <strong>vitamins A, B complex </strong>(esp. folic acid, B-6, and B12)<strong>, D, E, K, essential amino and fatty acids </strong>(ex. tryptophan affects serotonin levels and low cholesterol associated with mental disorders)<strong>, carbohydrates, low glucose </strong>(with associated diabetes)<strong>, calcium, magnesium, phosphorus, copper, electrolytes, l-carnitine, and inositrol, and selenium </strong>(1,5,8,9,38,55,56).</p>
<h3><strong>Symptoms</strong></h3>
<p>The <strong>etiology and pathogenesis</strong> of psychological disorders and cognitive symptoms in CD/gluten sensitivities is unclear. It is reasonable to suspect that immunological reactions, inflammation, various neurological&#160; abnormalities, and nutrient deficiencies may be responsible for the wide variety of psychological and cognitive symptoms. As well, enhanced production of cytokines in CD may stimulate the brain to produce neuroimmune, neuroendocrine, and neurochemical changes that may influence behavior. <strong>Pathological findings</strong> may include abnormal brain waves on electroencephalography (EEG), unusual cerebellar physiology, hypoperfused brain regions (also autoantibodies interferring with angiogenesis), brain atrophy, inflammation, patchy Purkinje cell (out-put neurons) loss in the cerebellum, and and progressive multifocal leukoencephalopathy (leading to destruction of myelin sheaths). As well, lymphocytic infiltration of the brain (along with associated vasculitis) could lead to glial, neuronal, or axonal damage. Other findings include widespread IgA deposition around vessels in the brain and brain white-matter lesions or calcifications, likely resulting from autoimmune reactions, calcium deposits, ischemia, vasculitis, or inflammatory demyelination (1,23,26,42,50-53,57-81). Collectively or individually, these factors may contribute to many psychological and cognitive symptoms. Many with undiagnosed CD (or gluten sensitivities) do not experience any psychological symptoms. </p>
<p>There are books, articles, and studies that identify an association between CD, gluten sensitivities, and <strong>depression</strong> ( 1,5,6,14,15,19,20,28,29,32,34,38,41,42-49,50-54,93). It is reasonable to suspect the central nervous system damage and inflammation combined with nutrient deficiencies (ex. low B vitamins, low serotonin and cholesterol) may be responsible. Other factors such as a sense of helplessness associated with being ill, misdiagnosed, or only having one’s symptoms diagnosed can certainly add to these feelings. Once diagnosed, depression might continue if underlying nutrient deficiencies are left untreated and unrecognized, if accidental ingestion of gluten occurs, if underlying food allergens are not identified, or if the individual has difficulty adjusting to a new lifestyle.&#160; As well, personal coping strategies, adequate support and follow-up from healthcare professionals, family and friend supports, availability of gluten-free food and resources can all influence the outcome<b> (1,38,22).</b></p>
<p><strong>Learning disabilities</strong> are associated with undiagnosed CD (1,10-12,23,27,40,42). In books, articles, and studies, <strong>Attention Deficit Disorder (ADD) And Attention-Deficit/Hyperactivity Disorder (ADHD)</strong> is also associated with CD and gluten sensitivity (13,24,25,27,42). As well, subtle or obvious cognitive decline,<strong> dementia</strong>, can be linked to CD and gluten sensitivity (58,60,91,132). This could have long lasting effects on one’s life, affecting their confidence, self esteem, and can also decrease an individual’s ability to pursue the career of their choice since the cognitive effects may lead to poor academic performance. </p>
<p>In studies and articles, other psychological disorders have been associated with undiagnosed CD and gluten sensitivities, such as <strong>schizophrenia spectrum disorders</strong> (17,18,37,38,39,55,56,94-99), <strong>anxiety problems</strong> (1,32,33), <strong>mood disorders</strong> (14), <strong>apathy</strong> (33), <strong>sitophobia (abnormal aversion to food) </strong>(33), <strong>irritability</strong> (33,42), <strong>obsessional neurosis</strong> (38), <strong>anorexia/bulimia</strong> (33,42), and <strong>delinquent behavior</strong> (14,15,38). As well, there has been much controversy questioning a link between gluten and A<strong>utism and/or Asperger’s</strong> <strong>Syndrome</strong>. There are many reasons for this, I may compile a follow-up post at a later date on this topic. It certainly appears as if many have intestinal involvement, it seems reasonable to suspect that gluten, casein, and other possible food antigens may be involved. For now, I’ve provided links to more information at the end of the post.</p>
<p><em>I often felt like it was <strong>difficult to think, learn, and analyze</strong>. I managed to graduate from University with Honors. However, I was studying constantly to achieve that. I couldn’t seem to retain information very well. Now that I’m eating gluten-free, (along with corn, rice, and diary-free) my head finally feels clear and I can analyse and retain information with greater ease. I feel like it only takes about 1/3 of the time&#160; to study now. It is difficult to learn when you are living with “<strong>Brain Fog</strong>”. My daughter, with CD, won an academic award last year. It may have been a very different outcome if she was still undiagnosed. She did have evidence of “brain fog” prior to diagnosis.</em></p>
<p><em>My middle child tested negative for CD. She had eczema<strong> </strong>of moderate severity, <strong>hyperactivity, lack of focus</strong>, occasional diarrhea, and abdominal discomfort. I was worried that she was experiencing some symptoms of ADHD. All medical tests ordered by the paediatric allergist were negative. An elimination diet revealed that she was sensitive to corn derivatives (which are in most grocery store products). All symptoms resolved when I removed corn from her diet. All symptoms return with accidental ingestion of corn derivatives. The hyperactivity and lack of focus is very pronounced with accidental ingestion of corn derivatives (ex. corn syrup, dextrose, glucose/fructose) which are in most processed foods.</em></p>
<p><strong>Note:</strong> <strong>For more information, go to the links at the end of this post.</strong></p>
<h3><strong>Influencing Factors</strong> </h3>
<p>Other factors that may add to psychological and cognitive symptoms include hypothyroidism, adrenal disorders, diabetes, infections, low oxygen levels, hypotension, epilepsy, sleep disorders, genetics, a traumatic event, certain medications, poor diet, vitamin deficiency or toxicity, lack of resources, alcoholism, heavy metals, solvents, street drugs, and gastric surgery (leading to deficiencies) (1,2,3,8,9).</p>
<h3><strong>Diagnosis</strong></h3>
<p>There are a number of tests to consider when diagnosing gluten sensitivities. IgA endomysial antibodies and IgA anti-transglutaminase 2</strong> tend to correspond with the severity of intestinal damage and is valuable along with an <strong>upper endoscopy</strong> <strong>with multiple biopsies</strong> to investigate intestinal involvement (1,5,6,82). <strong>Antibodies against deamidated gluten</strong> should be added to the celiac screen as well (83,100). If the patient has <strong>IgA deficiency then IgG tissue transglutaminase</strong> <strong>antibody test</strong> may be helpful. As well, <strong>IgG and IgA antigliadin antibodies</strong> may be helpful to identify if increased intestinal permeability has allowed gluten (gliadin) to leak in through the tight junctions between the intestinal epithelial cells. This leakage could potentially lead to a gluten sensitivity and with continued exposure potentially CD. Positive IgG and IgA antigliadin antibodies can indicate that a gluten sensitivity exists (1,5,6,64,84).  <strong>Anti-transglutaminase 6 IgA and IgG antibodies</strong> is prevalent in gluten ataxia and is useful to screen for gluten sensitivity in neurological disease (82). In a 2008 study, Dr. Hadjivassiliou (neurologist) and colleagues recommend anti-transglutaminase 6 IgG and IgA, HLA genetic testing, IgG and IgA anti-gliadin antibodies, and anti-transglutaminase 2 antibodies to help identify gluten sensitivities in individuals with neurological disease (85).</p>
<p>Additional tests are available as well such as fecal tests, rectal mucosal patch technique (new in Sweden), and genetic  tests. An MRI along with other neurological tests and biopsies may be ordered to investigate the pathological damage (1,5,6,78,86). It is important to explore the presence of nutrient deficiencies as well. </p>
<h3><strong>Do You Have Any Of The Above Symptoms?</strong></h3>
<p>CD can be present in children that are growing normally so normal growth rate should not be a factor that excludes the possibility of CD (87). Many individuals with undiagnosed CD/gluten sensitivities will have no bowel symptoms. Weight loss may or may not occur, and is dependent on the amount of the intestine that is damaged (1,2,3,9,88-90). Therefore, the symptoms in this post could occur in the absence of stunted growth, weight loss, or bowel symptoms.</p>
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<p>The presence of psychological and cognitive symptoms as discussed in this post, indicates that you should <strong>talk to your MD about</strong> <strong>tests for gluten sensitivities/CD and tests to rule out other possible causes of your symptoms.</strong> Testing for CD/gluten sensitivities is important because undiagnosed CD increases the risk of developing other autoimmune diseases, lymphomas (skin, brain, lymph nodes, intestine), cancers (thyroid, esophageal, mouth, tongue, pharynx, tonsil, and small intestine), allergies, complications from malabsorption issues, possible decreased immune response to other illnesses (1,2,5,6,91), and many other health complications that will be discussed in the posts about CD/gluten sensitivity symptoms. It is my hope that if you have psychological or cognitive symptoms, you can print out this post complete with medical references to take with you to the MD when you request testing. Highlight or underline the sections that apply to your symptoms. I’ll be posting a simplified summary and checklist in the 12th post.</p>
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<p>It is possible to have a gluten sensitivity even if you test negative for CD. It is also possible that some of your symptoms could be due to a food allergy/sensitivity or other disease process. For example, Dr. Stephen Wangen (<b><a href="http://tinyurl.com/yjsrqle)">http://tinyurl.com/yjsrqle)</a></b> describes how a boy with TIC disorder benefited&#160; a gluten-free, dairy-free diet (92). Allergy testing, and/or an elimination diet may help you to identify offending foods. Other tests can help rule out other diseases. I encourage everyone to have their symptoms thoroughly investigated by their MD and specialists before implementing a therapeutic diet. A consultation with a Registered Dietitian can provide guidance to ensure all nutritional needs are met. Keep your MD informed about any dietary changes you are making and also the results. Of course, I would love to hear your story as well.</p>
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<p><strong>I </strong><strong>recommend waiting until CD/gluten sensitivity testing is complete before initiating a gluten-free diet because it may create a false negative. Discuss this with your MD or specialist. <strong>USE CAUTION WITH SUPPLEMENTS. </strong>Toxicities can occur with over supplementation and this can lead to permanent damage. Consult your MD, Registered Dietitian, or other medical specialists involved in your care to determine which nutrients should be supplemented and to identify appropriate dosages for you.</strong> <strong>Review your symptoms and everything in this post with a Medical Doctor</strong> <strong>and your specialists before you make any changes</strong>. <strong>Your MD knows your medical history and the treatments that are appropriate for you.</strong></p>
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<p><strong>D</strong><strong>iagnosed Celiacs and people with food allergies/sensitivities</strong>, please comment about your symptoms&#160; and experiences at the end of each post. This will help other readers to see how the sometimes illusive symptoms of CD or food sensitivities can affect each of us.&#160; We are all unique!</p>
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<h3><strong>Links to more Information</strong></h3>
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<p>1. Dr. Scot Lewey. Celiac Disease and gluten linked to brain disease by deposits in intestine and brain. <b><a href="http://tinyurl.com/yje7nv5">http://tinyurl.com/yje7nv5</a></b> </p>
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<p>2. Dr. David Perlmutter, MD, FACN, ABIHM. Gluten sensitivity (Celiac Disease), ADHD, and other neurological problems in children. <b><a href="http://tinyurl.com/c2pzoo">http://tinyurl.com/c2pzoo</a></b> </p>
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<p>3. Niederhofer H, Pittschieler K. A preliminary investigation of ADHD Symptoms In persons With celiac Disease.&#160; <a title="http://jad.sagepub.com/cgi/content/abstract/10/2/200" href="http://jad.sagepub.com/cgi/content/abstract/10/2/200">http://jad.sagepub.com/cgi/content/abstract/10/2/200</a></p>
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<p>4. Nathanel Zelnik MD, Avi Pacht MD, Raid Obeid MD, Aaron Lerner MD. Range of Neurological Disorders In Patients With Celiac Disease.&#160; <b><a href="http://tinyurl.com/yjwaqrp">http://tinyurl.com/yjwaqrp</a></b> </p>
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<p>5. Elaine Gottschall. Recognizing Celiac behavior and catching it early by using SCD™ &#8211; would it prevent Autism? <a title="http://www.breakingtheviciouscycle.info/autism/dr_hass_exerpt.htm" href="http://www.breakingtheviciouscycle.info/autism/dr_hass_exerpt.htm">http://www.breakingtheviciouscycle.info/autism/dr_hass_exerpt.htm</a></p>
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<p>6. Dr. Vikki Peterson. D.C., C.C.N. Gluten Sensitivity And Depression. <b><a href="http://tinyurl.com/bl7ox3">http://tinyurl.com/bl7ox3</a></b> </p>
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<p>7. <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Ciacci%20C%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Ciacci C</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Iovino%20P%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Iovino P</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Amoruso%20D%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Amoruso D</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Siniscalchi%20M%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Siniscalchi M</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Tortora%20R%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Tortora R</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Di%20Gilio%20A%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Di Gilio A</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Fusco%20M%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Fusco M</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Mazzacca%20G%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstract">Mazzacca G</a>. Grown-up Coeliac Children: The Effects Of Only A Few Years On A Gluten-Free Diet In Childhood. <a title="http://www.ncbi.nlm.nih.gov/pubmed/15709993" href="http://www.ncbi.nlm.nih.gov/pubmed/15709993">http://www.ncbi.nlm.nih.gov/pubmed/15709993</a></p>
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<p>8. The gluten connection: the association between schizophrenia and celiac disease. <strong>&#160;&#160; <a title="http://www3.interscience.wiley.com/journal/118626206/abstract" href="http://www3.interscience.wiley.com/journal/118626206/abstract">http://www3.interscience.wiley.com/journal/118626206/abstract</a></strong>&#160; </p>
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<p>9. Findings in this study suggest that immune reactions in the intestine may affect individuals cognitively.&#160; A J Wakefield FRCS<sup><a href="http://www.nature.com/ajg/journal/v95/n9/abs/ajg2000579a.html#aff1"></a></sup> et el. Enterocolitis in children with developmental disorders. <a title="http://www.nature.com/ajg/journal/v95/n9/abs/ajg2000579a.html" href="http://www.nature.com/ajg/journal/v95/n9/abs/ajg2000579a.html">http://www.nature.com/ajg/journal/v95/n9/abs/ajg2000579a.html</a></p>
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<p>10. Ron Hoggan. Memory/Learning: Eating to Learn: How Grains Impact on Our Ability to Focus, Comprehend, Remember, Predict, and Survive. <b><a href="http://tinyurl.com/4nr67d">http://tinyurl.com/4nr67d</a></b> </p>
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<p>11. Prof. Rodney Ford M.B., B.S., M.D., F.R.A.C.P. Gluten Causes Brain Disease! <b><a href="http://tinyurl.com/naqvg9">http://tinyurl.com/naqvg9</a></b> </p>
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<p>12. Wendy Cohan, RN. Gluten, Celiac Disease and the Brain. <b><a href="http://tinyurl.com/d4z4c6">http://tinyurl.com/d4z4c6</a></b> </p>
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<p>13. Ron Hoggan. ADD, Attention Deficit Hyperactivity Disorder &#8211; ADHD and Celiac Disease. <b><a href="http://tinyurl.com/ll9tpw">http://tinyurl.com/ll9tpw</a></b> </p>
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<p>14. PA Pynnonen et el. Untreated Celiac Disease And Development Of Mental Disorders In Children And Adolescents.&#160;&#160; <a title="http://psy.psychiatryonline.org/cgi/reprint/43/4/331.pdf" href="http://psy.psychiatryonline.org/cgi/reprint/43/4/331.pdf">http://psy.psychiatryonline.org/cgi/reprint/43/4/331.pdf</a>&#160; </p>
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<p>15. Cholesterol is often low in undiagnosed Celiacs. Could the behaviour in this study be due to undiagnosed CD? Total serum cholesterol level, violent criminal offences, suicidal behaviour, mortality and the appearance of conduct disorder in Finnish male criminal offenders with antisocial personality disorder.&#160; <a title="http://www.ncbi.nlm.nih.gov/pubmed/12056583" href="http://www.ncbi.nlm.nih.gov/pubmed/12056583">http://www.ncbi.nlm.nih.gov/pubmed/12056583</a></p>
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<p>16. Cholesterol is often low in undiagnosed Celiacs. Could the behaviour in this study be due to undiagnosed CD?&#160; Association of Serum Cholesterol and History of School Suspension among School-age Children and Adolescents in the United States. <a title="http://aje.oxfordjournals.org/cgi/content/abstract/161/7/691" href="http://aje.oxfordjournals.org/cgi/content/abstract/161/7/691">http://aje.oxfordjournals.org/cgi/content/abstract/161/7/691</a></p>
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<p>17. Low Cholesterol and Mental Disorders in Children and Adolescents With Celiac Disease. <a title="http://psy.psychiatryonline.org/cgi/content/full/50/3/300" href="http://psy.psychiatryonline.org/cgi/content/full/50/3/300">http://psy.psychiatryonline.org/cgi/content/full/50/3/300</a></p>
<p>18.  Part 1: Video (case study) about the neurological presentation of Celiac Disease in a baby. http://www.youtube.com/watch?v=Am6AUFVpKUk&#038;NR=1</dt>
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<p>19. Part 2: Video (case study) about the neurological presentation of Celiac Disease in the same child as he became a toddler and preschooler. http://www.youtube.com/watch?v=TL_O-uInv3U&#038;feature=related</dt>
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<h3><strong>Links for Autism </strong></h3>
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<p>If you think your child may have CD/gluten sensitivities or other food sensitivities, consult your doctor for testing. A consultation with an Allergist for allergy testing may help to identify other allergies. A consultation with a Registered Dietician may help to ensure nutrient requirements are being met. </p>
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<p>1. Substitutive and dietetic approaches in childhood autistic disorder: interests and limits”. <a title="http://www.ncbi.nlm.nih.gov/pubmed/19068339" href="http://www.ncbi.nlm.nih.gov/pubmed/19068339">http://www.ncbi.nlm.nih.gov/pubmed/19068339</a></p>
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<p>2. Enterocolitis in children with developmental disorders.&#160; <a title="http://www.nature.com/ajg/journal/v95/n9/abs/ajg2000579a.html" href="http://www.nature.com/ajg/journal/v95/n9/abs/ajg2000579a.html">http://www.nature.com/ajg/journal/v95/n9/abs/ajg2000579a.html</a></p>
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<p>3. Wendy Cohan, RN. Gluten, Celiac Disease and the Brain. <b><a href="http://tinyurl.com/d4z4c6">http://tinyurl.com/d4z4c6</a></b> </p>
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<p>4. Autistic disorder and gastrointestinal disease.&#160; <a title="http://www.ncbi.nlm.nih.gov/pubmed/12352252?dopt=Abstract" href="http://www.ncbi.nlm.nih.gov/pubmed/12352252?dopt=Abstract">http://www.ncbi.nlm.nih.gov/pubmed/12352252?dopt=Abstract</a></p>
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<p>5. Panenteric IBD-Like Disease in a Patient with Regressive Autism Shown for the First Time by the Wireless Capsule Enteroscopy: Another Piece in the Jigsaw of this Gut-Brain Syndrome? <a title="http://www3.interscience.wiley.com/journal/118681866/abstract" href="http://www3.interscience.wiley.com/journal/118681866/abstract">http://www3.interscience.wiley.com/journal/118681866/abstract</a></p>
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<p>6. Focal-Enhanced Gastritis in Regressive Autism with Features Distinct from Crohn&#8217;s and Helicobacter Pylori Gastritis. <a title="http://www3.interscience.wiley.com/journal/118744704/abstract" href="http://www3.interscience.wiley.com/journal/118744704/abstract">http://www3.interscience.wiley.com/journal/118744704/abstract</a></p>
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<p>7. The intestinal lesion of autistic spectrum disorder. <a title="http://www.ncbi.nlm.nih.gov/pubmed/16003130?dopt=Abstract" href="http://www.ncbi.nlm.nih.gov/pubmed/16003130?dopt=Abstract">http://www.ncbi.nlm.nih.gov/pubmed/16003130?dopt=Abstract</a></p>
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<p>8. Differences between the gut microflora of children with autistic spectrum disorders and that of healthy children. <a title="http://www.ncbi.nlm.nih.gov/pubmed/16157555?dopt=Abstract" href="http://www.ncbi.nlm.nih.gov/pubmed/16157555?dopt=Abstract">http://www.ncbi.nlm.nih.gov/pubmed/16157555?dopt=Abstract</a></p>
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<p>9. Oxidative stress in autism. <b><a href="http://tinyurl.com/yfwf6mh">http://tinyurl.com/yfwf6mh</a></b>&#160;</p>
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<p>10. A Randomised, Controlled Study of Dietary Intervention in Autistic Syndromes. <a title="http://www.ncbi.nlm.nih.gov/pubmed/12168688" href="http://www.ncbi.nlm.nih.gov/pubmed/12168688">http://www.ncbi.nlm.nih.gov/pubmed/12168688</a>&#160; </p>
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<p>11. Can the pathophysiology of autism be explained by the nature of the discovered urine peptides? <a title="http://www.ncbi.nlm.nih.gov/pubmed/12608733" href="http://www.ncbi.nlm.nih.gov/pubmed/12608733">http://www.ncbi.nlm.nih.gov/pubmed/12608733</a></p>
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<p>12. Immune response to dietary proteins, gliadin and cerebellar peptides in children with autism. <a title="http://www.ncbi.nlm.nih.gov/pubmed/15526989" href="http://www.ncbi.nlm.nih.gov/pubmed/15526989">http://www.ncbi.nlm.nih.gov/pubmed/15526989</a></p>
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13. Jenny McCarthy http://www.generationrescue.org/autism/  and http://www.generationrescue.org/ </p>
<h3><strong>References</strong></h3>
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<h3><strong></strong></h3>
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<p>1. <cite><strong>Excellent Book:</strong> Green PHR, Jones, R. Celiac Disease A Hidden Epidemic. Collins, Harper Collins Publishers, 2006 <b><a href="http://tinyurl.com/ljeqjc">http://tinyurl.com/ljeqjc</a> </b></cite></p>
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<p><cite></cite><cite>2. </cite>Pruessner Harold T, MD. Detecting Celiac Disease In Your Patients. American Family Physician. March 1st, 1998.</p>
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<p>3. Feldman Mark, MD, Friedman Lawrence S, MD, Sleisenger, Marvin H, MD, Gastrointestinal and Liver Disease Pathophysiology/Diagnosis/Management 7th Edition, Volume11, 2002,Saunders</p>
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<p>4. Barrett KE. Gastrointestinal Physiology. Lange Medical Books/McGraw-Hill 2006.</p>
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<p>5. <strong>Excellent Book:</strong> Lieberman Shari PhD,CNC, FACN, with Linda Segall. The Gluten Connection. How Gluten Sensitivity May Be Sabotaging Your Health. Rodale Inc., 2007. <b><a href="http://tinyurl.com/nwsc79">http://tinyurl.com/nwsc79</a> </b></p>
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<p>6. <strong>Excellent Book:</strong> James Braly, MD., Ron Hoggan, MA. Dangerous Grains. Penguin Group, Inc., 2002. <b><a href="http://tinyurl.com/knswhn">http://tinyurl.com/knswhn</a></b>&#160;</p>
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<p>7. Medicinenet.com. How Are Malabsorption And Malnutrition Evaluated In Celiac Disease. <a title="http://www.medicinenet.com/celiac_disease/page7.htm#tocp" href="http://www.medicinenet.com/celiac_disease/page7.htm#tocp">http://www.medicinenet.com/celiac_disease/page7.htm#tocp</a></p>
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<p>8. Gibney MJ, Marinos E, Olle L, Dowsett J. Clinical Nutrition. Blackwell Publishing 2005.</p>
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<p>9. Gibney MJ, Vorster HH, Kok FJ. Introduction to Human Nutrition. Blackwell Publishing 2002.</p>
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<p>10. Ron Hoggan. Memory/Learning: Eating to Learn: How Grains Impact on Our Ability to Focus, Comprehend, Remember, Predict, and Survive. <a title="http://www.celiac.com/articles/711/1/MemoryLearning-Eating-to-Learn-How-Grains-Impact-on-Our-Ability-to-Focus-Comprehend-Remember-Predict-and-Survive-by-Ron-Hoggan/Page1.html" href="http://www.celiac.com/articles/711/1/MemoryLearning-Eating-to-Learn-How-Grains-Impact-on-Our-Ability-to-Focus-Comprehend-Remember-Predict-and-Survive-by-Ron-Hoggan/Page1.html">http://www.celiac.com/articles/711/1/MemoryLearning-Eating-to-Learn-How-Grains-Impact-on-Our-Ability-to-Focus-Comprehend-Remember-Predict-and-Survive-by-Ron-Hoggan/Page1.html</a></p>
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<p>99. GRAFF H, HANDFORD A.Celiac syndrome in the case histories of five schizophreics.&#160;&#160; Psychiatr Q. 1961 Apr;35:306-13.</p>
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100. S. Rashtak, M. Ettore, H. Homburger, J. Murray. Comparative Usefulness of Deamidated Gliadin Antibodies in the Diagnosis of Celiac Disease. Clinical Gastroenterology and Hepatology, Volume 6, Issue 4, Pages 426-432.</p>
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		<title>Part 8 Of 12 Part Series: Neurological Symptoms (Ataxia, Neuropathies, Seizures, Strokes, Migraines, Myopathies, Dementia) With Undiagnosed Celiac Disease, Gluten Intolerance or Sensitivities</title>
		<link>http://celiacnurse.com/neurological-symptoms-ataxia-neuropathies-seizures-strokes-migraines-myopathies-dementia-associated-with-undiagnosed-celiac-disease-gluten-intolerance-or-sensitivities/</link>
		<comments>http://celiacnurse.com/neurological-symptoms-ataxia-neuropathies-seizures-strokes-migraines-myopathies-dementia-associated-with-undiagnosed-celiac-disease-gluten-intolerance-or-sensitivities/#comments</comments>
		<pubDate>Fri, 13 Nov 2009 20:01:10 +0000</pubDate>
		<dc:creator>Shelly</dc:creator>
				<category><![CDATA[12 Part Series: CD Symptoms]]></category>

		<guid isPermaLink="false">http://celiacnurse.com/neurological-symptoms-ataxia-neuropathies-seizures-strokes-migraines-myopathies-dementia-associated-with-undiagnosed-celiac-disease-gluten-intolerance-or-sensitivities/</guid>
		<description><![CDATA[This is the eighth in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, neurological symptoms will be discussed. There are studies, articles, and books identifying an association between gluten intolerance/CD, gluten sensitivities, and neurological symptoms (1-3,5-13,16-110,115,117,119,120,136-144,148,151-153). The pathogenesis is thought to be [...]]]></description>
			<content:encoded><![CDATA[<p>This is the eighth in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, neurological symptoms will be discussed. There are studies, articles, and books identifying an association between gluten intolerance/CD, gluten sensitivities, and neurological symptoms (1-3,5-13,16-110,115,117,119,120,136-144,148,151-153). The pathogenesis is thought to be due to autoimmune reactions (to ingested gluten) causing inflammation and damage in the central and peripheral nervous systems in genetically predisposed individuals (1,17,18,21,23,24,29,30,71,83,110,117,118,123,152,153,155).<br />
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<p>Some <strong>abnormal findings</strong> can include abnormal brain waves on electroencephalography (EEG), unusual cerebellar physiology, hypoperfused brain regions, brain atrophy, inflammation, patchy Purkinje cell (out-put neurons) loss in the cerebellum, and and progressive multifocal leukoencephalopathy leading to destruction of myelin sheaths that support neuronal impulses. Other findings include lymphocytic infiltration of the cerebellum and peripheral nerves, damage to the posterior columns of the spinal cord, and widespread IgA deposition around vessels in the brain. As well, brain white-matter lesions or calcifications, likely resulting from autoimmune reactions, calcium deposits, ischemia, vasculitis, or inflammatory demyelination, can occur (1,10,16,19,26,38,56,58,67,73-76,99,100,105,107,111-116,118,151).</p>
<p>Many with neurological symptoms, associated with CD/gluten intolerances/gluten sensitivities, do not have bowel symptoms. In others, the intestinal villi responsible for absorbing nutrients becomes damaged, creating a flattened mucosal surface (villous flattening). Autoimmune reactions to ingested gluten and related prolamines cross-react with intestinal villi and create this damage. Various nutrient deficiencies can occur and this can cause or add to the severity of the neurological symptoms (1-4,7,11,14,15,59).&#160; <strong>Nutrient deficiencies</strong> contributing to neurological symptoms can include <strong>vitamins E, B complex, K, amino and fatty acids, calcium, magnesium, phosphorus, copper, electrolytes, l-carnitine, and inositrol </strong>(7,11-14,15,59,93,99).</p>
<h3><strong>Symptoms</strong></h3>
<p>Collectively, immunological reactions, various neurological&#160; abnormalities, and nutrient deficiencies can lead to a wide variety of neurological symptoms.</p>
<h4><strong>Gluten Ataxia</strong></h4>
<p><strong></strong>Gluten Ataxia may result from immunological damage to the cerebellum, posterior columns of the spinal cord, and peripheral nerves. Ataxia symptoms can include <strong>staggering gait, lack of balance, poor coordination, unsteadiness with standing or walking, increased falls, and dysarthric speech (may be slurred, slow, and difficult to produce and also the pitch, rhythm, loudness, and other voice qualities may change). Other symptoms include dysphagia (difficulty swallowing), clumsy exaggerated imprecise limb (arms and legs) movements, difficulty with fine-motor skills (ex. writing, buttoning a shirt, or eating),&#160; oculomotor (abnormal eye movements) problems, sensorimotor axonal neuropathy and other peripheral neuropathies. As well, dysmetria (inability to judge distance or scale), decreased processing of sensory information, sometimes declining cognitive function, and decreased cerebellar processing of afferent information (information from muscles, joints, movement, visual, auditory, somatosensory, cerebral cortex and midbrain) can occur.</strong> The progression of symptoms is generally slow. However, in some cases the progression is quick with cerebellar atrophy that can occur within 1 year of the initial symptom. A gluten-free diet may take a year or more to eliminate antibodies and this along with correction of nutrient deficiencies will hopefully decrease or stop further progression of symptoms. If permanent damage has already occurred, symptoms may not resolve. Children and infants can have ataxia symptoms as well (17,21,22,23,29,31,49,71,126,150,154).</p>
<h4><strong>Neuropathies (Neuritis)</strong></h4>
<p>Autoimmune damage to the nerves, inflammation, and nutrient deficiencies may lead to a variety of neuropathies. Symptoms can include <strong>burning, tingling, numbness, vibrations, pinching, stabbing, buzzing, pressure, muscle twitches, or a loss of feeling. These sensations can spread from an initial localized area to other parts of the body. Pain may also occur and may feel like an electric shock, legs may feel heavy, an increased sensitivity to touch may occur and paresthesias resulting in sensory loss and muscle weakness can occur. Other symptoms can include carpal tunnel syndrome, vestibular dysfunction (dizziness, lack of balance), myelitis, reduced reflexes, deep sensory loss, proprioceptive (sense of position in space) loss, dysesthesias (abnormal sensations), feeling like you are wearing gloves or stockings, difficulty moving limbs, frequently dropping items, walking with a wide stance (to compensate), and increased falls. As well, a change in bowel habits, sexual dysfunction, skin problems, organ dysfunction, </strong><strong>internuclear opthalmoplegia, myelopathies, paralysis, and acute paraplegia might occur.</strong> Autonomic nerve damage can also cause<strong> low blood pressure and dizziness</strong>. Onset can be sudden or gradual and neuropathies can affect any age (70,80,81,120,127)</p>
<p><em>I had intermittent tingling, numbness, vibrations, cold and burning feelings, and pain in my head, face, arms, and legs. I also had carpel tunnel for awhile and had to wear a brace. My daughter had tingling and numbness in her feet. Occasionally, I also experienced pressure on top of my head or on an extremity, and transient head and mouth numbness would occur. There were occasions where I actually felt like I was slurring my speech.</em></p>
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<h4><strong>Epilepsy (Seizures)</strong></h4>
<p>There is mystery regarding the pathogenesis of gluten-sensitive epilepsy, however, a connection between CD, bilateral occipital cerebral calcification (may or may not be present), and seizures has been noted. It is reasonable to suspect that immunological autoimmune reactions, possibly associated vasculitis, inflammation, and nutrient deficiencies may be responsible. The prognosis is influenced by how soon in the disease a gluten free diet is started. Seizure symptoms <strong>can include auras (perceptual disturbance prior to seizure), prodromes (ex. early symptom such as disorientation, <strong>photosensitivity, euphoria, or aphagia), loss of consciousness,&#160; automatisms (involuntary movements), versive (forced<sup> </sup>and involuntary head movements) or nonversive (mild, seemingly voluntary head movements). Other symptoms include confusion, vomiting, convulsions, difficulty</strong> talking, drooling, incontinence, temporary paralysis, sweating, and tachycardia (increased pulse). Involuntary movements during the seizure may include chewing movements, lip smacking, eyelid fluttering, eyes rolling up, falling, hand waving, stomping feet, may bit tongue, vocal sounds, shaking, stiffening, staring, swallowing, grinding and clenching teeth, tremors, and tensing muscles, altered breathing pattern, and twitching movements. Seizures may be grand mal, petit mal or focal. Immediate assessment by an MD can help rule out a stroke. (13,14,19,31,32,37-45,66,94,99,102,103,128,155).</strong></p>
<h4><strong>Migraines/Headaches</strong></h4>
<p><strong></strong>Episodic, mild to severe headaches, often with some form of transient neurological deficit, is associated with gluten sensitivities. Immunological reactions, inflammation, associated vasculitis, brain white matter, hypoperfused brain regions, altered brain waves, and nutrient deficiencies may contribute to this symptom. A <strong>pre-migraine/headache aura can occur and symptoms may include seeing spots, wavy lines, flashing lights, visual distortion of objects, weakness, numbness, confusion, difficulty with words, and/or a feeling of pins and needles. The migraine/headache symptoms may include pain in part or all of the head that is throbbing, pulsating, or stabbing, possibly with temporary visual loss or change (ocular migraine), nausea or vomiting, and sensitivity to light noise and smell. A complicated headache may involve extra symptoms, such as difficulty understanding speech, difficulty speaking, numbness, tingling, paralysis of a limb, or include another nervous system deficit (</strong>25,29,93,32-34,36,84,86,87,101,129,151). Be careful about assuming these symptoms are related to a headache since a stroke may cause similar symptoms. </p>
<p><em>I experienced ocular migraines.</em>&#160;<em>I would have partial vision loss, usually unilaterally, that would last 1-2 hours, then resolve. Occasionally, I would see flashes of light out of the corner of my eye, the room would seem cloudy, and I would see dots blocking my view, or dots of grey falling from the sky, like snow.</em> I had a full-check up with an optometrist and an ophthalmologist, but all tests were negative. Food allergies or sensitivities can cause neurological symptoms as well. Ten to twenty minutes after eating a banana, the roof of my mouth becomes very itchy, and my vision becomes blurred (usually without head discomfort) for 2-3 hours.&#160; </p>
<h4><strong>Cerebral Infarction (Strokes) and Thrombosis (Clots) Formation</strong></h4>
<p>Antiphospholipid Syndrome is associated with CD and this can increase the risk for arterial and venous thrombus formation (61,134,135). In a case study, three patients with CD had antiphospholipid syndrome. One experienced fetal death, the second case presented with thrombosis in her limb and had renal infarction. The third case had two spontaneous abortions and a transient ischemic cerebral attack (61). You can see how the presence of antiphospholipid syndrome in CD could possibly lead to strokes, renal problems, fetal complications, pulmonary emboli, heart attacks, or ischemic attacks in other areas of the body. Thrombosis, leading to ischemia could be the first symptom/diagnosis present in CD. Other factors that may contribute to stroke or thrombus formation include associated systemic vasculitis (leading to stenosis, occlusions, or aneurism of the blood vessels) or the activity of autoantibodies inhibiting angiogenesis (affecting the health of blood vessels). As well, vitamin K deficiency (due to malabsorption in CD) may increase the risk for an intracerebral bleed or cause a protein S and protein C deficiency possibly leading to thrombosis (21,29,60,96,125,155-158).&#160; Collectively or in isolation, these factors could lead to a variety of ischemic symptoms. </p>
<p>In case studies, strokes in children and adults were linked to CD (77-80). With a stroke, brain function is lost, as a result of ischemia, due to a thrombosis, embolism, or a hemorrhage. Stroke symptoms are dependent on the area of the brain that is compromised. Collectively, the symptoms may include <strong>convulsions, apneic attacks, difficulty swallowing, reduced vibratory and sensory sensation, decreased ability to move extremities (arms and legs) on one side of the body (hemiplegia) or paralysis, weakness, difficulty understanding or formulating speech (aphasia), visual field changes or defects, facial weakness, numbness, and decreased reflexes (swallow, gag, pupil reactions to light are altered ). Other symptoms include tongue weakness (may be unable to protrude or move side to side), sptosis (drooping of eyelid), ocular (eye) muscle weakness, sensory changes (hearing, taste, smell, vision touch), difficulty walking, difficulty with coordination, dizziness, incontinence, difficulty with balance, and nystagmus (involuntary eye movement). As well, abnormal breathing and heart rate, sternocleidomastoid muscle weakness (difficulty turning head to one side), apraxia (voluntary movements are altered), loss of memory, hemineglect, confusion, disorganized thinking, anosognosia (denial of a deficit), loss of consciousness, vomiting, and headache can occur</strong> (33,77-80,130,131). Permanent damage can occur. Thrombosis symptoms could also include <strong>organ failure, deep vein thrombosis, heart attack, or pulmonary emboli</strong>.</p>
<h4><strong>Myopathies</strong></h4>
<p>Muscle symptoms may result from immunological reactions affecting the nerves or muscle tissue, a compromised blood supply to the muscles, intramuscular bleeding, and/or nutrient deficiencies. <strong>Muscular symptoms can include cramps, stiffness, spasms, weakness, aching, pain, fatigue, swallowing difficulties (dysphagia), droopy eyelids, difficulty moving eyes, eye paralysis, limb weakness, weakness after exertion, tetany, decreased mobility, difficulty climbing stairs, difficulty breathing, myocarditis, hypotonia, decreased muscle mass, difficulty lifting objects or doing activities of daily living (3,12,13,38-46,48,49,56,59-63,65-70,93).</strong> If CD tests are negative, keep in mind that muscular symptoms can occur with gluten sensitivities, food allergies or sensitivities in the absence of CD. Gluten and dairy were specifically mentioned as possible antigens to try eliminating from one’s diet (48,49,58,76). An allergist or naturopathic doctor may be helpful to identify offending foods.</p>
<p>Myopathy involves a disease process that leads to dysfunctional muscle fibres. Various myopathies have been associated with CD and gluten sensitivity including <strong>dermatomyositis, polymyositis, inclusion body myositis, rhabdomyolysis, ocular myopathy, muscular dystrophy, neutrophillic myositis, muscular hypotonia of the infant or child, proximal myopathy and generalized myopathy</strong> (12,13,38-46,48,49,59-63,65-70,93). Intramuscular hemorrhage was also identified in one case study and this symptom was due to a vitamin K deficiency (75).</p>
<p><strong>Nutrient deficiencies</strong> (common in CD) that may contribute to muscular symptoms include vitamins <strong>A, D, E, K, niacin, thiamine, pantothenic</strong> <strong>acid, pyridoxine, <strong>cobalamin, </strong>protein, fat, carbohydrates, calcium, magnesium, phosporus, potassium, iodine, iron, and copper</strong> (14,15).</p>
<p><em>I experienced muscle cramps, stiffness, weakness, aching, and fatigue. There were times I felt so weak that I had to sit or lie down for awhile. My daughter and mother both had muscle cramps.</em></p>
<h4><strong>Dementia</strong></h4>
<p>Immunological reactions leading to brain atrophy, nerve damage, nutrient deficiencies, hypoperfused brain regions, vasculitis, and white matter lesions may contribute to dementia symptoms<strong>. </strong>Dementia can be very subtle or obvious. Dementia symptoms <strong>may include loss of short term memory, difficulty with finding words, memory loss or forgetfulness (ex. forgetting names or appointments), difficulty doing familiar tasks, personality or mood changes, change in behavior, and poor judgement. Other symptoms include paranoia, hallucinations, suspiciousness, confusion, disorientation in new or usual surroundings, difficulty with activities of daily living, altered sleep habits, difficulty learning, increased falls, aggressiveness, and inappropriate sexual behavior. As well, poor concentration, confabulation, anxiety, impaired swallowing, withdrawal from others, malnutrition (forget to eat), dehydration, seizures, injuries, difficulty with communication, poor organization, decreased motor and coordination function, personality changes, and difficulty reasoning can occur (58,60,91,132).</strong></p>
<p><em>Prior to diagnosis, I would experience foggy thinking and memory lapses.</em></p>
<p><em>Note: Psychological and other cognitive symptoms will be discussed in the next post. If you have any of the above symptoms, seek medical attention immediately for an assessment.</em></p>
<h3><strong>Other Contributing Factors</strong></h3>
<p>Other factors that may contribute to neurological symptoms include smoking, hypertension, diabetes, hyperlipidemia, ischemic heart disease, atrial fibrillation (potential for clots), hyperhomocysteinemia (associated with CD), renal failure, thyroid disease, calcium metabolism, inborn error of metabolism, trauma, infections, genetics, toxic-metabolic agents, certain medications, poor diet, vitamin deficiency or toxicity, alcoholism, heavy metals, solvents, street drugs, and gastric surgery (leading to deficiencies) (46,96,107).</p>
<h3><strong>Associated Conditions</strong></h3>
<p>In studies, CD and gluten-sensitivity is associated with other neurological diseases, such as Huntington’s Disease/Chorea (29,46,47,133), Ramsay Hunt Syndrome (28,69), Plummer Vinson Syndrome/Patterson Brown Kelly (8,9,81,82), Stiff Person Syndrome (29,104), and Multiple Sclerosis (MS) (85,136-143).</p>
<p>Gluten intolerance/sensitivities can produce a variety of neurological symptoms so it is reasonable to suspect that associated autoimmune damage, inflammation, and possible nutrient deficiencies may play a role in other autoimmune diseases such as Parkinson’s Disease, Amyotrophic Lateral Sclerosis (ALS)/Lou Gehrig’s Disease, Guillain–Barré Syndrome (GBS), or numerous other neurological conditions. If gluten sensitivity isn’t the culprit, then perhaps other various food antigens or processing agents are prompting an autoimmune response. </p>
<p>In individuals that are genetically predisposed to gluten sensitivities, gluten consumption can lead to <strong>increased expression of zonulin </strong>(a human protein that is a haptoglobin 2 precursor) in the intestinal tissues. This <strong>increases intestinal permeability</strong> allowing macromolecules (ex. food antigens, bacterial, and viral particles) exposure to the immune system. The immune systems exposure to gluten and the subsequent autoimmune reaction is thought to be responsible for the intestinal and other systemic damage seen in Celiac Disease. Unfortunately, the <strong>increased bowel permeability can also increase the risk of developing food allergies/intolerances/sensitivities.</strong> Dr. Alessio Fasano and his research team feel this is part of the underlying pathogenesis involved in CD and possibly many other autoimmune diseases. Could increased intestinal permeability, leading to immune exposure to many possible food antigens, be responsible for other neurological diseases such as Parkinson’s Disease, ALS and Guillain–Barré Syndrome? (109).</p>
<p>Wendy Cohen (Registered Nurse), wrote an interesting article “Is There A Link Between Parkinson’s Disease And Gluten Intolerance” (<b><a href="http://tinyurl.com/y8tamew">http://tinyurl.com/y8tamew</a></b> Ref-92). Wendy makes some interesting observations which highlight the possibility of gluten possibly playing a role in Parkinson’s Disease. As with Parkinson’s Disease, I am curious about a possible link between ALS, gluten intolerances and other food allergens. My grandfather had ALS. My mother (his daughter), myself, and my daughter have CD. Could my grandfather have been misdiagnosed? Did he really have neurological and muscular symptoms as a result of undiagnosed CD?&#160; One article, identified a 44 year old male who was misdiagnosed with ALS. Further investigation 6 months later revealed that he really had CD. He was put on a gluten-free diet and 9 months later his symptoms had improved (148). The abstract can be viewed at <a title="http://www.ncbi.nlm.nih.gov/pubmed/17914346" href="http://www.ncbi.nlm.nih.gov/pubmed/17914346">http://www.ncbi.nlm.nih.gov/pubmed/17914346</a> and the case summary <a title="http://www.medscape.com/viewarticle/563701" href="http://www.medscape.com/viewarticle/563701">http://www.medscape.com/viewarticle/563701</a>. </p>
<p>Another area of interest, is the use of Palaeolithic diets to lesson immune responses and control symptoms. Theoretically, this may help many with symptoms related to food intolerances since all grains, dairy, legumes, and processed sugar (eliminates corn sweeteners too) are removed from the diet. With this diet, individuals eat very primal foods, with the belief that our bodies may have difficulty immunologically with foods that have been introduced fairly recently in our evolutionary history. A researcher, Dr. Loren Cordain, PhD, (from Colorado State University, USA) discusses the use of a Palaeolithic diet for Multiple Sclerosis in a 2007 video, “Potential Therapeutic Characteristics of Pre-agricultural Diets In The Prevention And Treatment Of Multiple Sclerosis” <a title="http://wildhorse.insinc.com/directms03oct2007/" href="http://wildhorse.insinc.com/directms03oct2007/">http://wildhorse.insinc.com/directms03oct2007/</a>. Dr. Cordain discusses how 4 individuals with MS benefited from this diet and believes this diet may benefit others with various autoimmune diseases as well. I have a friend with MS. Upon diagnosis, her neurologist recommended a gluten-free and casein free diet. She feels that this diet has helped to control her symptoms. I wonder if a Paleolithic diet would completely halt the disease. The video is located on Ashton Embry&#8217;s website at Direct-MS. </p>
<p>More research is needed to investigate possible links between food antigens and other neurological diseases. A therapeutic diet would be an attractive alternative to the use of medications (with possible side effects) and other possibly invasive procedures. Further research, better diagnostic tests, and increased awareness can help medical professionals and patients put the pieces of the gluten/food sensitivity puzzle together. If you feel you may benefit from a gluten-free, grain–free, or Paleolithic diet, talk to your doctor and a Registered Dietitian for advise.</p>
<h3><strong>Diagnosis</strong></h3>
<p>There are a number of tests to consider when diagnosing gluten sensitivities. <strong>IgA endomysial antibodies and IgA anti-transglutaminase 2</strong> tend to correspond with the severity of intestinal damage and is valuable along with an <strong>upper endoscopy</strong> <strong>with multiple biopsies</strong> to investigate intestinal involvement (1,5,6,152). Antibodies against deamidated gluten is another test that should be added to the screening process (147,160,161). If the patient has <strong>IgA deficiency then IgG tissue transglutaminase</strong> <strong>antibody test</strong> may be helpful. As well, <strong>IgG and IgA antigliadin antibodies</strong> may be helpful to identify if increased intestinal permeability has allowed gluten (gliadin) to leak in through the tight junctions between the intestinal epithelial cells. This leakage could potentially lead to a gluten sensitivity and with continued exposure potentially CD. Positive IgG and/or IgA antigliadin antibodies can indicate that a gluten sensitivity exists (1,5,6,51-54,57,58,106,119). <strong>Anti-transglutaminase 6 IgA and IgG antibodies</strong> is prevalent in gluten ataxia and is useful to screen for gluten sensitivity in neurological disease. In a 2008 study, Dr. Hadjivassiliou (neurologist) and colleagues recommend anti-transglutaminase 6 IgG and IgA, HLA genetic testing, IgG and IgA anti-gliadin antibodies, and anti-transglutaminase 2 antibodies to help identify gluten sensitivities in individuals with neurological disease (145). I noticed online that Elisa-kits are available from <a href="http://tgase.org/resources/content/pdf/newsletter_200806.pdf">Zedira</a> for anti-transglutaminase 6 IgA and IgG antibodies. Discuss this with your doctor before ordering as the test might be available locally at your lab and I don&#8217;t know that much about this company </p>
<p>Additional tests are available as well such as fecal tests, rectal mucosal patch technique (new in Sweden), and genetic tests. An MRI along with other neurological tests and biopsies may be ordered to investigate the pathological damage (1,5,6,115,146). Tests may reveal other autoantibodies are involved such as anti-ganglioside antibodies, anti-Purkinje cell antibodies, anti-glutamic acid decarboxylase (GAD), anti-synapsin antibodies and other anti-neuronal antibodies. As well, oligoclonal bands may be present in the cerebral spinal fluid (118,122,123,153). It is important to explore the presence of nutrient deficiencies as well. </p>
<h3><strong>Do You Have Any Of The Above Symptoms?</strong></h3>
<p>CD can be present in children that are growing normally so normal growth rate should not be a factor that excludes the possibility of CD (159). Many individuals with undiagnosed CD/gluten sensitivities will have no bowel symptoms. Weight loss may or may not occur, and is dependent on the amount of the intestine that is damaged (1,15,29,30,71,106). Therefore, the symptoms in this post could occur in the absence of stunted growth, weight loss, or bowel symptoms.</p>
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<p>The presence of neurological symptoms as discussed in this post, indicates that you should <strong>talk to your MD about</strong> <strong>tests for gluten sensitivities/CD and tests to rule out other possible causes of your symptoms.</strong> Testing for CD/gluten sensitivities is important because undiagnosed CD increases the risk of developing other autoimmune diseases, lymphomas (skin, brain, lymph nodes, intestine), cancers (thyroid, esophageal, mouth, tongue, pharynx, tonsil, and small intestine), allergies, complications from malabsorption issues, possible decreased immune response to other illnesses (1,2,5,6,109), and many other health complications that will be discussed in the posts about CD/gluten sensitivity symptoms. It is my hope that if you have neuromuscular symptoms you can print out this post complete with medical references to take with you to the MD when you request testing. Highlight or underline the sections that apply to your symptoms. I’ll be posting a simplified summary and checklist in the 12th post.</p>
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<p>It is possible to have a gluten sensitivity even if you test negative for CD. It is also possible that some of your symptoms could be due to a food allergy/sensitivity or other disease process. For example, Dr. Stephen Wangen (<b><a href="http://tinyurl.com/yjsrqle)">http://tinyurl.com/yjsrqle)</a></b> describes how a boy with TIC disorder benefited&#160; a gluten-free, dairy-free diet (95). Allergy testing, and/or an elimination diet may help you to identify offending foods. Other tests can help rule out other diseases. I encourage everyone to have their symptoms thoroughly investigated by their MD and specialists before implementing a therapeutic diet. A consultation with a Registered Dietician can provide guidance to ensure all nutritional needs are met. Keep your MD informed about any dietary changes you are making and also the results. Of course, I would love to hear your story as well.</p>
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<p><strong>I </strong><strong>recommend waiting until CD/gluten sensitivity testing is complete before initiating a gluten-free diet because it may create a false negative. Discuss this with your MD or specialist. <strong>USE CAUTION WITH SUPPLEMENTS. </strong>Toxicities can occur with over supplementation and this can lead to permanent damage. Consult your MD, Registered Dietitian, or other medical specialists involved in your care to determine which nutrients should be supplemented and to identify appropriate dosages for you.</strong> <strong>Review your symptoms and everything in this post with a Medical Doctor</strong> <strong>and your specialists before you make any changes</strong>. <strong>Your MD knows your medical history and the treatments that are appropriate for you.</strong></p>
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<p><strong>D</strong><strong>iagnosed Celiacs and people with food allergies/sensitivities</strong>, please comment about your symptoms&#160; and experiences at the end of each post. This will help other readers to see how the sometimes illusive symptoms of CD or food sensitivities can affect each of us.&#160; We are all unique!</p>
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<h3><strong>References</strong></h3>
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<p>1. <cite><strong>Excellent Book:</strong> Green PHR, Jones, R. Celiac Disease A Hidden Epidemic. Collins, Harper Collins Publishers, 2006 <b>http://tinyurl.com/ljeqjc </b></cite></p>
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<p><cite></cite><cite>2. </cite>Pruessner Harold T, MD. Detecting Celiac Disease In Your Patients. American Family Physician. March 1st, 1998.</p>
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<p>3. Feldman Mark, MD, Friedman Lawrence S, MD, Sleisenger, Marvin H, MD, Gastrointestinal and Liver Disease Pathophysiology/Diagnosis/Management 7th Edition, Volume11, 2002,Saunders</p>
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<p>4. Barrett KE. Gastrointestinal Physiology. Lange Medical Books/McGraw-Hill 2006.</p>
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<p>5. <strong>Excellent Book:</strong> Lieberman Shari PhD,CNC, FACN, with Linda Segall. The Gluten Connection. How Gluten Sensitivity May Be Sabotaging Your Health. Rodale Inc., 2007. <b>http://tinyurl.com/nwsc79 </b></p>
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<p>6. <strong>Excellent Book:</strong> James Braly, MD., Ron Hoggan, MA. Dangerous Grains. Penguin Group, Inc., 2002. http://tinyurl.com/knswhn  </p>
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<p>7. Ackerman Z, Eliashiv S, Reches A, Zimmerman J. Neurological manifestations in celiac disease and vitamin E deficiency. J Clin Gastroenterol. 1989 Oct;11(5):603–605</p>
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<p>8. Hoffman RM, Jaffe PE. Plummer-Vinson syndrome. A case report and literature review. Arch Intern Med. 1995;155:2008-2011. </p>
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<p>9. Dickey W, McConnell B. Celiac disease presenting as the Paterson-Brown Kelly (Plummer-Vinson) syndrome. Am J Gastroenterol. 1999;94:527-529.</p>
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<p>10. Hadjivassiliou M, Grunewald RA, Chattopadhyay AK, Davies-Jones GA, Gibson A, Jarrat JA, et el. Clinical, Radiological, Neurophysiological, And Neuropathological Characteristics Of Gluten Ataxia. Lancet 1998;352:1582-5.</p>
<p>11. Henri-Bhargava Alexandre, Melmed Calvin, Glikstein Rafael, and Schipper Hyman M. NEUROLOGIC IMPAIRMENT DUE TO VITAMIN E AND COPPER DEFICIENCIES IN CELIAC DISEASE. Neurology, Vol. 71, Issue 11, 860-861, September 9, 2008</p>
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<p>84. Adams Jefferson. Children with Migraines May Face Higher Risk for Celiac Disease. <a href="http://www.celiac.com">www.celiac.com</a>&#160; <a title="http://www.celiac.com/articles/21656/1/Children-with-Migraines-May-Face-Higher-Risk-for-Celiac-Disease/Page1.html" href="http://www.celiac.com/articles/21656/1/Children-with-Migraines-May-Face-Higher-Risk-for-Celiac-Disease/Page1.html">http://www.celiac.com/articles/21656/1/Children-with-Migraines-May-Face-Higher-Risk-for-Celiac-Disease/Page1.html</a></p>
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<p>85. Adams Scott. Multiple Sclerosis and Celiac Disease. <a href="http://www.celiac.com">www.celiac.com</a> <a title="http://www.celiac.com/categories/Celiac-Disease-Research:-Associated-Diseases-and-Disorders/Multiple-Sclerosis-and-Celiac-Disease/" href="http://www.celiac.com/categories/Celiac-Disease-Research:-Associated-Diseases-and-Disorders/Multiple-Sclerosis-and-Celiac-Disease/">http://www.celiac.com/categories/Celiac-Disease-Research:-Associated-Diseases-and-Disorders/Multiple-Sclerosis-and-Celiac-Disease/</a>&#160; He provides additional links.</p>
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<p>89. Adams Scott. Celiac Neuropathy Should be Considered when Neuropathy has Unknown Origin. <a href="http://www.celiac.com">www.celiac.com</a> <a title="http://www.celiac.com/articles/625/1/Celiac-Neuropathy-Should-be-Considered-when-Neuropathy-has-Unknown-Origin/Page1.html" href="http://www.celiac.com/articles/625/1/Celiac-Neuropathy-Should-be-Considered-when-Neuropathy-has-Unknown-Origin/Page1.html">http://www.celiac.com/articles/625/1/Celiac-Neuropathy-Should-be-Considered-when-Neuropathy-has-Unknown-Origin/Page1.html</a></p>
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<p>151. Maurizio GabrielliM.D. <sup>a</sup> , Filippo CremoniniM.D. <sup>a</sup> , Giuseppe FioreM.D. <sup>b,</sup> <sup>c</sup> , Giovanni AddoloratoM.D <sup>b,</sup> <sup>c</sup> , Cristiano PadalinoM.D <sup>b,</sup> <sup>c</sup> , Marcello CandelliM.D <sup>b,</sup> <sup>c</sup> , Maria Elena De LeoM.D <sup>b,</sup> <sup>c</sup> , Luca SantarelliM.D <sup>b,</sup> <sup>c</sup> , Mario GiacovazzoM.D <sup>b,</sup> <sup>c</sup> , Antonio GasbarriniM.D <sup>b,</sup> <sup>c</sup> , Paolo PolaM.D <sup>b,</sup> <sup>c</sup> , Antonio GasbarriniM.D. Association Between Migraine and Celiac Disease: Results From a Preliminary Case-Control and Therapeutic Study. <a href="http://www3.interscience.wiley.com/journal/117955841/home">The American Journal of Gastroenterology</a>&#160; Volume 98 Issue 3,&#160; 2004,&#160; Pages 625 – 629.</p>
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		<title>Part 7 Of 12 Part Series: Urological Symptoms (Incontinence, Prostatitis, Interstitial Cystitis, Urethritis, IgA Nephropathy, Glomerulonephritis, Kidney Stones, Nephritis, Nephrotic Syndrome and Recurrent Bladder Infections) Associated With Undiagnosed Celiac Disease, A Gluten Sensitivity, Or A Food Allergy/Sensitivity</title>
		<link>http://celiacnurse.com/urological-symptoms-incontinence-prostatitis-interstitial-cystitis-urethritis-iga-nephropathy-glomerulonephritis-kidney-stones-nephritis-nephrotic-syndrome-and-recurrent-bladder-infections-a/</link>
		<comments>http://celiacnurse.com/urological-symptoms-incontinence-prostatitis-interstitial-cystitis-urethritis-iga-nephropathy-glomerulonephritis-kidney-stones-nephritis-nephrotic-syndrome-and-recurrent-bladder-infections-a/#comments</comments>
		<pubDate>Tue, 13 Oct 2009 16:56:10 +0000</pubDate>
		<dc:creator>Shelly</dc:creator>
				<category><![CDATA[12 Part Series: CD Symptoms]]></category>

		<guid isPermaLink="false">http://celiacnurse.com/urological-symptoms-incontinence-prostatitis-interstitial-cystitis-urethritis-iga-nephropathy-glomerulonephritis-kidney-stones-nephritis-nephrotic-syndrome-and-recurrent-bladder-infections-a/</guid>
		<description><![CDATA[This is the seventh in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, urological symptoms associated with undiagnosed CD, a gluten sensitivity, or food allergies/sensitivities will be discussed. Gluten Intolerance or Sensitivity There are studies and articles identifying an association between gluten [...]]]></description>
			<content:encoded><![CDATA[<p>This is the seventh in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, urological symptoms associated with undiagnosed CD, a gluten sensitivity, or food allergies/sensitivities will be discussed.<br />
<span id="more-145"></span>
</p>
<h3><strong>Gluten Intolerance or Sensitivity</strong></h3>
<p>There are studies and articles identifying an association between gluten intolerance/CD, gluten sensitivities, and urological symptoms (10-37,44-46,54). However, the <strong>pathogenesis</strong> of urological symptoms due to gluten consumption and the resulting autoimmune damage is unclear. Hypothetically, these symptoms may result from <strong>auto-antibodies</strong> directed at the kidneys, ureters, bladder, or the urethra. This is plausible since we know that auto-antibodies in CD (resulting from autoimmune reactions to ingested gluten) can cause damage to a variety of other bodily tissues such as the intestinal mucosa (villous flattening), muscles, nerves, skin, and liver. Additionally, if intestinal damage occurs (well researched), the flattened villi are less able to absorb nutrients leading to various <strong>nutrient deficiencies</strong> that may affect the urological system. We know that nutrient deficiencies can adversely affect muscle, nerve, and mucosal tissue so it is reasonable to expect that the urological system would be affected since it is dependent on these systems (1,2,3,47-50,52,53). A gluten sensitivity that has not progressed to the point of becoming obvious CD could also be responsible for urological symptoms since the same or similar immune system reactions would be occurring (28,29,32,40,45)</p>
<h3><strong>Food Allergies Or Sensitivities</strong></h3>
<p>Individuals with CD/gluten intolerance or gluten sensitivity are at a higher risk for allergies due to increased permeability of the intestine. In these individuals, gluten consumption can lead to <strong>increased expression of zonulin (a human protein) in the intestinal tissues. This increases intestinal permeability allowing macromolecules (ex. food antigens, bacterial, and viral particles) exposure to the immune system.</strong> The immune systems exposure to gluten and the subsequent autoimmune reaction is thought to be responsible for the intestinal and other systemic damage seen in Celiac Disease. Unfortunately, the <strong>increased bowel permeability can also increase the risk of developing food allergies/intolerances/sensitivities (9).</strong> If urological symptoms persist once diagnosed and gluten-free, then a food allergy or sensitivity may exist. In the absence of CD/gluten sensitivity, food allergies/sensitivities may be the sole or part of the underlying reason for your symptoms (8,28,32-34,35-43,45,46,54-56).</p>
<p>Various food <strong>allergies/sensitivities</strong> have been linked either through <strong>research, case studies, or personal experiences </strong>to urological symptoms (8,28,32-34,35-43,45,46,54-56). <strong>Dr. Gislason (MD)</strong> said in his book, Core Diet For Kids, “The mucosal surfaces of the bladder and vagina should be thought of as similar to the nose, throat, and gastrointestinal mucosa, with similar reactions to food allergens, circulating in the blood stream. If milk, wheat, and egg allergy can cause rhinitis, they can also result in vaginitis, urethritis, and cystitis” (8). Histamine and mast cells are involved in immune reactions to food and are involved in CD (64,65). <strong>Histamine has been detected in bladder washings and mucosal mast cells</strong> have been located in the detrusor muscle, lamina propria, and epithelium of the bladder in patients with interstitial cystitis (55,56). As well, the <strong>kidneys may be vulnerable to damage if exposed to immune complexes (resulting from reactions with food allergens) that are circulating in the blood</strong> since the kidney filters all the blood (8,54 ). It is reasonable to suspect that a reaction to food antigens may be responsible for immune reactions leading to many other urological conditions (10-46,54). </p>
<p>A <strong>few studies</strong> have examined the urological effects of food antigens. Various food allergens such as <strong>milk proteins</strong> (41,42), <strong>soy bean protein</strong> (36,42), <strong>rice protein</strong> (42), <strong>gliadin</strong> (in gluten) (19,20,24,33,34,36,39,40), <strong>oat flour extracts</strong> (36), <strong>ovalbumin</strong> (36,39), and <strong>bovine serum albumin</strong> (39) have been associated with urological symptoms. <strong>Increased intestinal permeability</strong> has been identified in IgA nephropathy (36,37). As described above, this could lead to an interaction between food molecules and the immune system possibly leading to an immune mediated reaction. More studies are needed to investigate the presence of increased intestinal permeability in other urological conditions. Future studies demonstrating this association could help prove that there is an increased risk for immune reactions to food in those with urological conditions. Other common food allergens that may cause an immune reaction include <strong>wheat, eggs, fish/seafood, tree nuts, sulphites, sesame seeds, peanuts, and corn</strong> (corn derivatives are in most grocery store products). <strong>Almost any food, pesticide, or food additive</strong> could cause an immune mediated reaction in the form of an allergy, intolerance, or sensitivity (8,63). <strong>Wendy Cohen (RN)</strong>&#160;<a href="http://www.wellbladder.com">www.wellbladder.com</a> identified <strong>caffeine, tomatoes, chocolate, alcohol, and citrus as possible bladder irritants</strong> (28). Wendy has many comments on her urology articles describing personal experiences with food intolerances and sensitivities (28,29,32,45). </p>
<p>If you suspect an allergy or sensitivity may be causing your symptoms, a consultation with an <strong>allergist and/or naturopathic doctor</strong> may be helpful. There are a variety of tests that are useful for identifying allergies and sensitivities. Some individuals use the core or elimination diet to do this. A <strong>Registered Dietitian</strong> can help to ensure all nutrient requirements are fulfilled. Other tests ordered by a <strong>medical doctor</strong> (MD) can help rule out other diseases. I encourage everyone to have their symptoms thoroughly investigated by their MD and specialists before implementing a therapeutic diet. Keep your MD informed about any dietary changes you are making and also the results. </p>
<p>More research is needed. Research results demonstrating an association between food allergens and urological symptoms could lead to dietary intervention as the key to primary prevention and treatment of many urological symptoms. Personal and healthcare benefits include <strong>decreased hospitalization, decreased physician visits, decreased use of medications, and increased quality of life for individuals suffering with urological symptoms.</strong></p>
<h3><strong>Symptoms</strong></h3>
<p>Urological symptoms may include <strong>chronic prostatitis, interstitial cystitis, bedwetting in children, stress incontinence, frequency and urgency to urinate, bladder spasms, chronic or recurrent bladder infections, urethritis, IgA nephropathy, nephrotic syndrome, kidney stones (renal calculus), active albuminuria, proteinuria, haematuria, glomerulonephritis, mesangial nephritis, glomerulitis, membranoproliferative glomerulonephritis, IgA mesangial glomerulonephritis, immunoglobulin A mesangial nephropathy, and midaortic syndrome affecting infrarenal aorta or renal arteries. </strong>Many of these conditions can lead to <strong>renal failure (2,8,10-46,54).</strong> Further research may reveal other symptoms or urological conditions such as renal rickets, neurogenic bladder, or polycystic kidney disease. Ron Hoggan (author in a book, “Dangerous Grains”) mentioned a woman with polycystic kidney disease and CD in one of his articles (54). <em>I also experienced frequent ovarian cysts prior to my diagnosis so it seems reasonable to suspect that cysts could occur elsewhere it the body. I do not have problems with ovarian cysts now.</em> <em>Prior to my diagnosis,&#160; I&#160; experienced occasional urine frequency and bladder cramping. The urine dipsticks and urine culture and sensitivity would surprisingly be negative. Perhaps this was due to bladder irritants, nutrient deficiencies (affecting the muscles, nerves,&#160; or mucosa) or other immune factors such as mast cells and histamine.</em></p>
<h3><strong>Possible Factors Causing False Negative CD Tests</strong></h3>
<p>The blood tests for CD (IgA endomysial antibodies and IgA tissue transglutaminase) tend to correspond with the severity of intestinal damage. Therefore, if the autoimmune damage is in another area (ex. skin form of CD called dermatitis herpetiformis or as discussed in this article, it could be the urological system) and no or very little intestinal damage is present, a negative result could occur. If the above tests are negative, a bloodtest for&#160; antigliadin antibodies may be helpful to identify if increased intestinal permeability has allowed gluten (gliadin) to leak in through the tight junctions between the intestinal epithelial cells. This leakage could potentially lead to a gluten sensitivity and with continued exposure potentially CD. Antibodies against deamidated gluten should be added to the screening as well (63). Additional tests are available as well such as fecal tests, rectal mucosal patch technique (new in Sweden), and genetic tests. Other causes of false negative CD tests could include IgA deficiency (IgG tissue transglutaminase antibody test may be helpful), low gluten consumption, or the intestinal biopsy may have missed the diseased mucosa since it can be patchy in nature (multiple biopsies can be helpful to avoid this) (1,5,6,51-54,54,57,58). </p>
<h3><strong>Nutrient Deficiencies</strong></h3>
<p>Nutrient deficiencies that may contribute to <strong>nerve related urological symptoms</strong> in the bladder may include <strong>vitamins E, B complex, amino and fatty acids, calcium, magnesium, phosphorus, copper, electrolytes, and inositrol</strong>. (58-62). </p>
<p>Nutrient deficiencies&#160; that may contribute to <strong>muscular related urological symptoms</strong> in the bladder may include vitamins <strong>A, D, E, K, niacin, thiamine, pantothenic</strong> <strong>acid, pyridoxine, <strong>cobalamin, amino and fatty acids, </strong>carbohydrates, calcium, magnesium, phosporus, potassium, iodine, iron, and copper</strong> (57-59).&#160; </p>
<p>Nutrients deficiencies that may affect <strong>urological</strong> <strong>mucosal health </strong>include <strong>vitamin A, B complex, C, D,E, K, amino and fatty acids, carbohydrates, iron, zinc, copper, manganese, and molybdenum (58,59).</strong></p>
<p><strong><strong>USE CAUTION WITH SUPPLEMENTS. </strong>Toxicities can occur with over supplementation (especially with urological conditions) and this can lead to permanent damage. Consult your MD, Registered Dietician, or other medical specialists involved in your care to determine which nutrients should be supplemented and to identify appropriate dosages for you.</strong>&#160;</p>
<h3><strong>Other factors Affecting Kidney Or Bladder Function</strong></h3>
<p>Other factors that may contribute to kidney and bladder symptoms include diabetes, hypotension, hypertension, poor diet, alcoholism, street drugs, past surgery, poor heart function, infections, protein toxicity, tumours, congenital defects, trauma, toxicity from chemicals, certain medications, or vitamin toxicity (58,59,66). </p>
<h3><strong>Do You Have Any Of The Above Symptoms?</strong></h3>
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<p><strong>CD can be present in preteen/adolescents that are growing normally so normal growth rate (height) should not be a factor that excludes the possibility of CD in those with delayed puberty (51). Many individuals with undiagnosed CD will have no bowel symptoms (3,7,48,50). Weight loss may or may not occur, and is dependent on the amount of the intestine that is damaged (3,50). Therefore, the symptoms in this post could occur in the absence of stunted growth, weight loss, or bowel symptoms.</strong></p>
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<p>The presence of urological symptoms as discussed in this post, indicates that you should <strong>talk to your MD about</strong> <strong>tests for CD, allergy tests, and tests to rule out other possible causes of your symptoms.</strong> Testing for CD is important because undiagnosed CD increases the risk of developing other autoimmune diseases, lymphomas (skin, brain, lymph nodes, intestine), cancers (thyroid, esophageal, mouth, tongue, pharynx, tonsil, and small intestine), allergies, complications from malabsorption issues, possible decreased immune response to other illnesses (1,2,5,6,9,47,48), and many other health complications that will be discussed in the posts about CD symptoms. It is my hope that if you have urological symptoms you can print out this post complete with medical references to take with you to the MD when you request a CD test. Highlight or underline the sections that apply to your symptoms. I’ll be posting a simplified summary and checklist in the 12th post.</p>
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<p><strong>I recommend waiting until CD testing is complete before initiating a gluten-free diet because it may create a false negative. Discuss this with your MD or specialist. </strong><strong>Review your symptoms and everything in this post with a Medical Doctor</strong> <strong>and your specialists before you make any changes</strong>. <strong>Your MD knows your medical history and the treatments that are appropriate for you.</strong></p>
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<h3><strong>Links To More Information </strong></h3>
<p><strong>1.</strong> <strong>Wendy Cohen RN</strong> </p>
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<p><strong>Gluten Sensitivity and Bladder Disease</strong>. <a href="http://tinyurl.com/4zx94e">http://tinyurl.com/4zx94e</a></p>
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<p><strong>Interstitial Cystitis and Gluten Intolerance.</strong> <a href="http://tinyurl.com/ydw7krc">http://tinyurl.com/ydw7krc</a></p>
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<p><strong>Bladder Symptoms &amp; Gluten Sensitivity</strong>. <a href="http://tinyurl.com/crtcjm">http://tinyurl.com/crtcjm</a></p>
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<p><strong>The Chronic Prostatitis And Celiac Disease Connection</strong>. <a href="http://tinyurl.com/ybdzsgp">http://tinyurl.com/ybdzsgp</a></p>
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<p><strong>2.</strong> <strong>Ron Hoggan (One author from book, “Dangerous Grains”</strong>) </p>
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<p><strong>Kidney Problems</strong>&#160; <a title="http://www.gluten-free.org/hoggan/kidneyceliac.txt" href="http://www.gluten-free.org/hoggan/kidneyceliac.txt">http://www.gluten-free.org/hoggan/kidneyceliac.txt</a></p>
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<p><strong>Kidney Stones</strong> <a title="http://www.gluten-free.org/hoggan/kidney.txt" href="http://www.gluten-free.org/hoggan/kidney.txt">http://www.gluten-free.org/hoggan/kidney.txt</a></p>
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<p><strong>Nephrotic Syndrome</strong> <a title="http://www.gluten-free.org/hoggan/nephrotic.txt" href="http://www.gluten-free.org/hoggan/nephrotic.txt">http://www.gluten-free.org/hoggan/nephrotic.txt</a></p>
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<p><strong>3.</strong> <strong>Adams Scott. Kidney Disease And Celiac Disease</strong>. <a href="http://www.celiac.com">www.celiac.com</a> <b><a href="http://tinyurl.com/yamwe7q">http://tinyurl.com/yamwe7q</a></b></p>
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<p><strong>4. Adams Jefferson. Celiac Patients Face Higher Risk of Developing Chronic Renal Disease.&#160; <a href="http://www.celiac.com">www.celiac.com</a> </strong><strong><b><a href="http://tinyurl.com/az6tol">http://tinyurl.com/az6tol</a></b></strong></p>
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<p><strong>5. Relationship between intestinal permeability and antibodies against food antigens in IgA nephropathy. <a href="http://tinyurl.com/yducynx">http://tinyurl.com/yducynx</a></strong></p>
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<p><strong>6. The pathogenetic potential of environmental antigens in IgA nephropathy. <a href="http://tinyurl.com/ydaw6yh">http://tinyurl.com/ydaw6yh</a></strong></p>
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<p><strong>7. Dietary antigens and primary immunoglobulin A nephropathy. <a href="http://tinyurl.com/yc5ehq5">http://tinyurl.com/yc5ehq5</a></strong></p>
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<p><strong>8. Glomerular deposition of food antigens in IgA nephropathy. <a href="http://tinyurl.com/ydowje9">http://tinyurl.com/ydowje9</a></strong></p>
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<p><strong>9. Mediterranean diet and primary IgA nephropathy. <a href="http://tinyurl.com/yemq8pg">http://tinyurl.com/yemq8pg</a></strong></p>
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<p><strong>10. Histamine and mucosal mast cells in interstitial cystitis. <a title="http://www.ncbi.nlm.nih.gov/pubmed/2750582" href="http://www.ncbi.nlm.nih.gov/pubmed/2750582">http://www.ncbi.nlm.nih.gov/pubmed/2750582</a>&#160;</strong></p>
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<p><strong>11. Interstitial Cystitis: Correlation with Nerve Fibres, Mast Cells and Histamine. <b><a href="http://tinyurl.com/yjsnpe2">http://tinyurl.com/yjsnpe2</a></b> </strong></p>
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<h2><strong>References</strong></h2>
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<p><cite>1. <strong>Excellent Book:</strong> Green PHR, Jones, R. Celiac Disease A Hidden Epidemic. Collins, Harper Collins Publishers, 2006 <b><a href="http://tinyurl.com/ljeqjc">http://tinyurl.com/ljeqjc</a> </b></cite></p>
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<p><cite></cite><cite>2. </cite>Pruessner Harold T, MD. Detecting Celiac Disease In Your Patients. American Family Physician. March 1st, 1998.</p>
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<p>3. Feldman Mark, MD, Friedman Lawrence S, MD, Sleisenger, Marvin H, MD, Gastrointestinal and Liver Disease Pathophysiology/Diagnosis/Management 7th Edition, Volume11, 2002,Saunders</p>
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<p>4. Barrett KE. Gastrointestinal Physiology. Lange Medical Books/McGraw-Hill 2006.</p>
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<p>5. <strong>Excellent Book:</strong> Lieberman Shari PhD,CNC, FACN, with Linda Segall. The Gluten Connection. How Gluten Sensitivity May Be Sabotaging Your Health. Rodale Inc., 2007. <b><a href="http://tinyurl.com/nwsc79">http://tinyurl.com/nwsc79</a> </b></p>
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<p>6. <strong>Excellent Book:</strong> James Braly, MD., Ron Hoggan, MA. Dangerous Grains. Penguin Group, Inc., 2002. <b><a href="http://tinyurl.com/knswhn">http://tinyurl.com/knswhn</a></b></p>
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<p><strong>7. </strong><strong>M Hadjivassiliou,</strong><strong><sup>a</sup></strong> <strong>A K Chattopadhyay,</strong><strong><sup>b</sup></strong> <strong>G A B Davies-Jones,</strong><strong><sup>a</sup></strong> <strong>A Gibson,</strong><strong><sup>a</sup></strong> <strong>R A Grünewald,</strong><strong><sup>a</sup></strong> <strong>A J Lobo</strong><strong><sup>c</sup></strong> Neuromuscular disorder as a presenting feature of coeliac disease. <i>J Neurol Neurosurg Psychiatry</i> 1997;<b>63:</b>770-775 ( December )</p>
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<p>8. Gislason Stephen, MD. Core Diet For Kids. Persona Audiovisual Productions, 1989. He started <a href="http://www.nutramed.com">www.nutramed.com</a> (I’m not sure if he still owns it).</p>
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<p>9. Alessio Fasano, M.D. Physiological, Pathological, and Therapeutic Implications of Zonulin-Mediated Intestinal Barrier Modulation. American Journal of Pathology, 2008;173:1243-1252.</p>
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<p>10. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Ostojska%20J%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Ostojska J</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Okni%C5%84ska-Hoffmann%20E%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Okni?ska-Hoffmann E</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Gutkowska%20J%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Gutkowska J</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Radzikowski%20A%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Radzikowski A</b></a>. Chronic urinary tract infection and celiac disease in children. <a href="http://www.ncbi.nlm.nih.gov/">Pediatr Pol.</a> 1979 Nov;54(11):1263-71.</p>
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<p>11. C. Ciacci, G. Spagnuolo, R. Tortora, C. Bucci, D. Franzese, F. Zingone, M. Cirillo. Urinary Stone Disease in Adults With Celiac Disease: Prevalence, Incidence and Urinary Determinants. <em>The Journal of Urology</em>, Volume 180, Issue 3, Pages 974-979</p>
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<p>12. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Gama%20R%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Gama R</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Schweitzer%20FA%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Schweitzer FA</b></a>. Renal calculus: a unique presentation of coeliac disease. <a href="http://www.ncbi.nlm.nih.gov/">BJU Int.</a> 1999 Sep;84(4):528-9.</p>
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<p>13. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Codaccioni%20JL%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Codaccioni JL</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Pierron%20H%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Pierron H</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Perrimond%20H%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Perrimond H</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Boyer%20J%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Boyer J</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Unal%20D%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Unal D</b></a>. Unusual development during a 1-year period of multiple complications (steatorrhea, nephropathy, statural retardation, cerebral accidents) in a 15-year-old child diabetic since the age of 4. <a href="http://www.ncbi.nlm.nih.gov/">abete.</a> 1968 Apr-Jun;16(2):146-52.</p>
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<p>14. Woodrow G, Innes A, Boyd SM, Burden RP. A Case Of IgA Nephropathy With Coeliac Disease Responding To A Gluten-free Diet. Nephrol Dial Transplant (1993) 8: 1382-1383.</p>
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<p>15. Kenar D. Jhaveri<sup>1</sup>, Vivette D. D’Agati<sup>2</sup>, Robert Pursell<sup>3</sup> and David Serur<sup>1,4</sup>&#160; Coeliac sprue-associated membranoproliferative glomerulonephritis (MPGN). <strong>NDT Advance Access published online on July 22, 2009 </strong>      <br />Nephrology Dialysis Transplantation, doi:10.1093/ndt/gfp353</p>
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<p>16. R Coppo, A Amore and D Roccatello. Dietary antigens and primary immunoglobulin A nephropathy. Journal of the American Society of Nephrology, Vol 2, S173-S180, Copyright © 1992 by American Society of Nephrology</p>
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<p>17. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Gaboardi%20F%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Gaboardi F</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Perletti%20L%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Perletti L</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Cambi%C3%A9%20M%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Cambié M</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Mihatsch%20MJ%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Mihatsch MJ</b></a>. Dermatitis herpetiformis and nephrotic syndrome. <a href="http://www.ncbi.nlm.nih.gov/">Clin Nephrol.</a> 1983 Jul;20(1):49-51.</p>
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<p>18. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Scholey%20J%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Scholey J</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Freeman%20HJ%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Freeman HJ</b></a>. Celiac sprue-associated immune complex glomerulonephritis. <a href="http://www.ncbi.nlm.nih.gov/">J Clin Gastroenterol.</a> 1986 Apr;8(2):181-3.</p>
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<p>19. Mai Ots<sup>a</sup>, Oivi Uibo<sup>b</sup>, Kaja Metsküla<sup>c</sup>, Raivo Uibo<sup>c</sup>, Vello Salupere<sup>a</sup>&#160; IgA-Antigliadin Antibodies in Patients with IgA Nephropathy: The Secondary Phenomenon? <i>Am J Nephrol</i> 1999;19:453-458 (DOI: 10.1159/000013497)</p>
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<p>20. Jérôme Laurent<sup>a</sup>, Anne Branellec<sup>a</sup>, Jean-Marie Heslan<sup>a</sup>, Guy Rostoker<sup>a</sup>, Charles Bruneau<sup>a</sup>, Chantal André<sup>b</sup>, Liliane Intrator<sup>b</sup>, Gilbert Lagrue<sup>a</sup>&#160; An Increase in Circulating IgA Antibodies to Gliadin in IgA Mesangial Glomerulonephritis. <i>Am J Nephrol</i> 1987;7:178-183 (DOI: 10.1159/000167460)</p>
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<p>49. Hadjivassiliou M, Gibson A, Davies-Jones GA, Lobo AJ, Stephenson TJ, Milford-Ward A. Does Cryptic Gluten Sensitivity Play A Part In Neurological Illness? Lancet. 1996 Feb. 10;347(8998):369-71.</p>
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<p>50. <strong>M Hadjivassiliou,</strong><strong><sup>a</sup></strong> <strong>A K Chattopadhyay,</strong><strong><sup>b</sup></strong> <strong>G A B Davies-Jones,</strong><strong><sup>a</sup></strong> <strong>A Gibson,</strong><strong><sup>a</sup></strong> <strong>R A Grünewald,</strong><strong><sup>a</sup></strong> <strong>A J Lobo</strong><strong><sup>c</sup></strong> Neuromuscular disorder as a presenting feature of coeliac disease. <i>J Neurol Neurosurg Psychiatry</i> 1997;<b>63:</b>770-775 ( December )</p>
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<p>51. Lejarraga H, et el. Normal Growth Velocity Before Diagnosis Of Celiac Disease. J Pediatr Gastrenterol Nutr 2000;30:552-556.</p>
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<p>52. Abenavoli L, Proietti I, Leggio L, Ferrulli A, Vonghia L, Capizzi R, Rotoli M, Amerio PL, Gasbarrini g, Addolorato G. Cutaneous Manifestations In Celiac disease. World Journal Of Gastroenterology. 2006 February 14;12(6):843-852.</p>
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<p>53. Devlin Shane MD, Andrews Christopher MD, beck Paul MD, Celiac Disease. CME Update May 2004.</p>
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<p>54. Ron Hoggan (from book “Dangerous Grains”) Articles (responses to questions)</p>
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<p>Kidney Problems&#160; <a title="http://www.gluten-free.org/hoggan/kidneyceliac.txt" href="http://www.gluten-free.org/hoggan/kidneyceliac.txt">http://www.gluten-free.org/hoggan/kidneyceliac.txt</a></p>
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<p>Kidney Stones <a title="http://www.gluten-free.org/hoggan/kidney.txt" href="http://www.gluten-free.org/hoggan/kidney.txt">http://www.gluten-free.org/hoggan/kidney.txt</a></p>
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<p>Nephrotic Syndrome <a title="http://www.gluten-free.org/hoggan/nephrotic.txt" href="http://www.gluten-free.org/hoggan/nephrotic.txt">http://www.gluten-free.org/hoggan/nephrotic.txt</a></p>
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<p>55. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Enerb%C3%A4ck%20L%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Enerbäck L</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Fall%20M%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Fall M</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Aldenborg%20F%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Aldenborg F</b></a>. Histamine and mucosal mast cells in interstitial cystitis. <a href="http://www.ncbi.nlm.nih.gov/">Agents Actions.</a> 1989 Apr;27(1-2):113-6.</p>
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<p>56. T. LUNDEBERG<sup>1,</sup><a href="http://www3.interscience.wiley.com/journal/121518282/abstract?CRETRY=1&amp;SRETRY=0#c1"><sup>2</sup></a>, H. LIEDBERG<sup>1</sup>, L. NORDLING<sup>1</sup>, E. THEODORSSON<sup>1</sup>, A. OWZARSKI<sup>1</sup> P. EKMAN<sup>1</sup> Interstitial Cystitis: Correlation with Nerve Fibres, Mast Cells and Histamine. <a href="http://www3.interscience.wiley.com/journal/119198717/home">British Journal of Urology</a>&#160;<strong><a href="http://www3.interscience.wiley.com/journal/121518273/issue">Volume 71 Issue 4</a>, Pages 427 – 429, 1998 British Journal of Urology. </strong><strong>Published Online: </strong>26 Nov 2008</p>
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<p>57. Chernoff Ronni. Geriatric Nutrition: The Health Professionals Handbook. Jones And Bartlett Publishers Inc. 3rd edition, 2006.</p>
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<p>58. Gibney MJ, Marinos E, Olle L, Dowsett J. Clinical Nutrition. Blackwell Publishing 2005.</p>
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<p>59. Gibney MJ, Vorster HH, Kok FJ. Introduction to Human Nutrition. Blackwell Publishing 2002.</p>
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<p>60. Henri-Bhargava Alexandre, Melmed Calvin, Glikstein Rafael, and Schipper Hyman M. NEUROLOGIC IMPAIRMENT DUE TO VITAMIN E AND COPPER DEFICIENCIES IN CELIAC DISEASE. Neurology, Vol. 71, Issue 11, 860-861, September 9, 2008</p>
<p>61. Mayo Clinic Staff. Peripheral Neuropathy. <a href="http://www.mayoclinic.com">www.mayoclinic.com</a></p>
<p>62. Dunlop William M., M.D.; James G. Watson , III, M.D., F.A.C.P.; and Hume David M. , M.D., F.A.C.S.<a name="RFN1"></a><sup>&#160;</sup> Anemia and Neutropenia Caused by Copper Deficiency. Annals of Internal medicine. 1 April 1974 | Volume 80 Issue 4 | Pages 470-476</p>
<p>63. S. Rashtak, M. Ettore, H. Homburger, J. Murray. Comparative Usefulness of Deamidated Gliadin Antibodies in the Diagnosis of Celiac Disease. Clinical Gastroenterology and Hepatology, Volume 6, Issue 4, Pages 426-432.</p>
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		<title>Part 6 Of 12 Part Series: Reproductive (Delayed Puberty, Amenorrhea, Infertility, Impotence, Chronic Pelvic Pain, Fetal Complications, Premature Birth, Miscarriages, And Early Menopause) Symptoms In Undiagnosed Celiac Disease</title>
		<link>http://celiacnurse.com/part-6-of-12-part-series-reproductive-delayed-puberty-amenorrhea-infertility-chronic-pelvic-pain-fetal-complications-miscarriages-and-early-menopause-symptoms-in-undiagnosed-celiac-disease/</link>
		<comments>http://celiacnurse.com/part-6-of-12-part-series-reproductive-delayed-puberty-amenorrhea-infertility-chronic-pelvic-pain-fetal-complications-miscarriages-and-early-menopause-symptoms-in-undiagnosed-celiac-disease/#comments</comments>
		<pubDate>Thu, 01 Oct 2009 19:13:12 +0000</pubDate>
		<dc:creator>Shelly</dc:creator>
				<category><![CDATA[12 Part Series: CD Symptoms]]></category>

		<guid isPermaLink="false">http://celiacnurse.com/part-6-of-12-part-series-reproductive-delayed-puberty-amenorrhea-infertility-chronic-pelvic-pain-fetal-complications-miscarriages-and-early-menopause-symptoms-in-undiagnosed-celiac-disease/</guid>
		<description><![CDATA[This is the sixth in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, reproductive symptoms associated with undiagnosed CD will be discussed. There are studies, articles, and books identifying an association between CD and reproductive symptoms (1-39). However, the pathogenesis of reproductive [...]]]></description>
			<content:encoded><![CDATA[<p>This is the sixth in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, reproductive symptoms associated with undiagnosed CD will be discussed.<br />
<span id="more-120"></span><br />
There are studies, articles, and books identifying an association between CD and reproductive symptoms (1-39). However, the pathogenesis of reproductive symptoms due to ingestion of gluten and the resulting autoimmune damage is unclear. Hypothetically, these symptoms may result from auto-antibodies directed at hormones, organs necessary for development in puberty, reproductive organs, or fetal tissue. This is plausible since we know that auto-antibodies in CD (resulting from autoimmune reactions to ingested gluten) can cause damage to a variety of bodily tissues such as the intestinal mucosa (villous flattening), muscles, nerves, skin, pancreas, and liver. Additionally, if intestinal damage occurs (well researched), the intestinal villi are less able to absorb nutrients leading to various nutrient deficiencies that may affect sex hormones, health of the reproductive organs, threaten the viability of a fetus, or decrease success with breast feeding. Collectively, these influencing factors are likely responsible for the reproductive symptoms evident in CD. Reproductive symptoms may be the first to develop in undiagnosed CD and can occur without bowel or other extra-intestinal symptoms (1,2,3,4,12,23,36,49,50,63,64).</p>
<h3><strong>Symptoms</strong></h3>
<p><strong>Reproductive symptoms may include</strong>&#160;<strong>hypogonadism, pubertal delay (failure to develop secondary sex characteristics), delayed or retarded menarche, secondary amenorrhea, chronic pelvic pain, dysmenorrhea (severe uterine menstral pain), dyspareunia (intercourse is painful), vaginal infections, vaginitis, decreased sex drive (decreased libido), impotence, sperm abnormalities, infertility (in men or women), preclampsia, miscarriages, zygote abnormalties, fetal complications (birth defects, intrauterine fetal growth restriction, lower birth weight, premature birth), abnormal bleeding or infections post birth in mother, poor breast milk quality and production, and early menopause (1-39). </strong>The sense of loss experienced by individuals with these symptoms can be overwhelming and psychologically scarring. Imagine the loss of reproductive years due to infertility, the loss of a baby, or dealing with birth defects (stress, worry), only to find out later that it was due to the ingestion of gluten. Diagnosis and the implementation of a gluten-free diet is key to the primary prevention of reproductive symptoms in those with CD. Unfortunately, diagnosis of CD can be delayed for years due to the elusive presentation of symptoms (1,49,50). </p>
<p><em>I was <strong>diagnosed at age 38</strong>. I didn’t suffer from infertility and had 3 children. I did have <strong>delayed menarche</strong> <strong>and also had some problems with my pregnancies.</strong> <strong>My first child</strong> was born 3 weeks early due to my water breaking and I had anemia and palpitations during the pregnancy. I did not have any intestinal symptoms (classic CD symptoms) until after the birth of my first child. I was told that I had irritable bowel syndrome (see my gastrointestinal post). With my <strong>second pregnancy</strong>, I was hospitalized and put on bedrest due to premature inter-uterine contractions and pain. I also had anemia with this pregnancy and delivered 2 weeks early. With my <strong>third pregnancy</strong>, I had inter-uterine fetal growth restriction and had to decrease my activity. I remember adding lots of pasta and bread into my diet to help increase weight (exactly the opposite of what I needed since the pasta and bread had a high gluten content). My third child was born 1 1/2 weeks early at 6 pounds, 6 ounces and did receive some assistance with breathing when she was born. <strong>My mother</strong> (diagnosed with CD at age 60) almost lost her second child due to pregnancy complications. </em></p>
<p><em>I breast fed all 3 babies. However, I had to stop breast feeding the third after six weeks due to poor breast milk quality and production. I was ill with bowel symptoms at that time and likely had multiple nutrient deficiencies. </em></p>
<p><em><strong>Note:</strong> Delivery of a baby by 2-3 weeks early is still considered full-term. However, I thought that the fact that all 3 children were born before their due date is worth mentioning. </em></p>
<h3><strong>Nutrient Deficiencies</strong> </h3>
<p>Nutrient deficiencies (common in CD) that may contribute to reproductive symptoms in CD include vitamins <strong>A,D,E</strong> <strong>K</strong>, <strong>B complex,</strong>&#160;<strong>C</strong>, <strong>essential amino and fatty acids, carbohydrates, iodine, electrolytes, calcium, magnesium, phosphorus, iron, copper,</strong> <strong>manganese, <strong>zinc</strong> and molybdenum</strong> (1,41-48). Severity of nutrient loss and related symptoms are dependent on the location, length and severity of intestinal villi damage, which can be patchy in nature, and the presence of other factors such as diarrhea, vomiting, medications that affect nutrient absorption, other associated diseases, intestinal parasites, a poor diet, past stomach and intestinal surgery, smoking, or alcoholism (1-3,36,41,42,49,50).</p>
<h3><strong>Do You Have Any Of The Above Symptoms?</strong></h3>
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<p><strong>CD can be present in preteen/adolescents that are growing normally so normal growth rate (height) should not be a factor that excludes the possibility of CD in those with delayed puberty (55). Many individuals with undiagnosed CD will have no bowel symptoms (3,50,52,56). Weight loss may or may not occur, and is dependent on the amount of the intestine that is damaged (3,56). Therefore, the symptoms in this post could occur in the absence of stunted growth, weight loss, or bowel symptoms.</strong></p>
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<p>The presence of reproductive symptoms as discussed in this post, indicates that you should <strong>talk to your MD about</strong> <strong>tests for CD and tests to rule out other possible causes of your symptoms.</strong> Testing for CD is important because undiagnosed CD increases the risk of developing other autoimmune diseases, lymphomas (skin, brain, lymph nodes, intestine), cancers (thyroid, esophageal, mouth, tongue, pharynx, tonsil, and small intestine), allergies, complications from malabsorption issues, possible decreased immune response to other illnesses (1,2,5,6,50,81), and many other health complications that will be discussed in the posts about CD symptoms. It is my hope that if you have reproductive symptoms you can print out this post complete with medical references to take with you to the MD when you request a CD test. Highlight or underline the sections that apply to your symptoms. I’ll be posting a simplified summary and checklist in the 12th post.</p>
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<p>There are factors that can cause a <strong>false negative CD test</strong>. The blood tests for CD (IgA endomysial antibodies and IgA tissue transglutaminase) tend to correspond with the severity of intestinal damage. Therefore, if the autoimmune damage is in another area (ex. skin form of CD called dermatitis herpetiformis) and no or very little intestinal damage is present, a negative result could occur. If the above tests are negative, a bloodtest for&#160; antigliadin antibodies may be helpful to identify if increased intestinal permeability has allowed gluten (gliadin) to leak in through the tight junctions between the intestinal epithelial cells. This leakage could potentially lead to a gluten sensitivity and with continued exposure, potentially CD. A positive antigliadin result suggests that a gluten sensitivity may exist and the individual may benefit from a gluten-free diet. Antibodies against deamidated gluten should be also be added to the screening (65). Additional tests are available as well such as fecal tests and genetic tests. Other causes of false negative CD tests could include IgA deficiency (IgG tissue transglutaminase antibody test may be helpful), low gluten consumption, or the intestinal biopsy may have missed the diseased mucosa since it can be patchy in nature (multiple biopsies can be helpful to avoid this) (1,5,6,51-54,54,57,58). </p>
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<p>It is also possible that some of your symptoms could be due to a <strong>food allergy/sensitivity</strong> or other disease process. A consultation with an allergist and/or naturopathic doctor may be helpful. There are a variety of tests that are useful for identifying allergies and sensitivities. Some individuals use the core or elimination diet to do this. A Registered Dietitian can help to ensure all nutrient requirements are fulfilled. Other tests can help rule out other diseases. I encourage everyone to have their symptoms thoroughly investigated by their MD and specialists before implementing a therapeutic diet. Keep your MD informed about any dietary changes you are making and also the results. Of course, I would love to hear your story as well (41,57-61).</p>
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<p>I recommend waiting until CD testing is complete before initiating a gluten-free diet because it may create a false negative. Discuss this with your MD or specialist. USE CAUTION WITH SUPPLEMENTS. Toxicities can occur with over supplementation and this can lead to permanent damage. Consult your MD, Registered Dietitian, or other medical specialists involved in your care to determine which nutrients should be supplemented and to identify appropriate dosages for you. Review your symptoms and everything in this post with a Medical Doctor and your specialists before you make any changes. Your MD knows your medical history and the treatments that are appropriate for you.</p>
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<h3><strong>References</strong></h3>
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<p><cite>1. <strong>Excellent Book:</strong> Green PHR, Jones, R. Celiac Disease A Hidden Epidemic. Collins, Harper Collins Publishers, 2006 <b><a href="http://tinyurl.com/ljeqjc">http://tinyurl.com/ljeqjc</a> </b></cite></p>
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<p><cite></cite><cite>2. </cite>Pruessner Harold T, MD. Detecting Celiac Disease In Your Patients. American Family Physician. March 1st, 1998.</p>
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<p>3. Feldman Mark, MD, Friedman Lawrence S, MD, Sleisenger, Marvin H, MD, Gastrointestinal and Liver Disease Pathophysiology/Diagnosis/Management 7th Edition, Volume11, 2002,Saunders</p>
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<p>4. Barrett KE. Gastrointestinal Physiology. Lange Medical Books/McGraw-Hill 2006.</p>
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<p>5. <strong>Excellent Book:</strong> Lieberman Shari PhD,CNC, FACN, with Linda Segall. The Gluten Connection. How Gluten Sensitivity May Be Sabotaging Your Health. Rodale Inc., 2007. <b><a href="http://tinyurl.com/nwsc79">http://tinyurl.com/nwsc79</a> </b></p>
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<p>6. <strong>Excellent Book:</strong> James Braly, MD., Ron Hoggan, MA. Dangerous Grains. Penguin Group, Inc., 2002. <b><a href="http://tinyurl.com/knswhn">http://tinyurl.com/knswhn</a></b></p>
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<p><strong>7.</strong> ELIAKIM Rami<sup> (1)</sup> ; SHERER David M.<sup> (2)</sup><strong> ; </strong>Celiac disease : Fertility and pregnancy.&#160; <sup>(1) </sup>Division of Gastroenterology, Rambam Medical Center, Technion School of Medicine, Haifa, ISRAEL. <sup>(2) </sup>Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, St. Luke&#8217;s-Roosevelt Hospital Center, University of Columbia College of Physicians and Surgeons, New York, N.Y., ETATS-UNIS. <a title="http://cat.inist.fr/?aModele=afficheN&amp;cpsidt=859066" href="http://cat.inist.fr/?aModele=afficheN&amp;cpsidt=859066">http://cat.inist.fr/?aModele=afficheN&amp;cpsidt=859066</a></p>
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<p>8. Rudolph Colin D., Rudolph Abraham M., Hostetter Margaret K., and Lister George E. <a href="http://www.amazon.ca/Rudolphs-Pediatrics-Colin-D-Rudolph/dp/0838582850/ref=sr_1_1?ie=UTF8&amp;s=books&amp;qid=1254161232&amp;sr=1-1">Rudolph&#8217;s Pediatrics</a>,&#160; McGraw-Hill Professional; 21 edition, 2002.</p>
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<p>9. Green-Hernandez Carol, Singleton Joanne K., and Aronzon Daniel Z . <a href="http://www.amazon.ca/Primary-Care-Pediatrics-Carol-Green-Hernandez/dp/0781720087/ref=sr_1_1?ie=UTF8&amp;s=books&amp;qid=1254161552&amp;sr=1-1">Primary Care Pediatrics</a> Lippincott Williams &amp; Wilkins; 1 edition (Jan 1 2001)</p>
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<p>10. Hudson Tori. <a href="http://www.amazon.ca/Womens-Encyclopedia-Natural-Medicine-Alternative/dp/0071464735/ref=sr_1_1?ie=UTF8&amp;s=books&amp;qid=1254161701&amp;sr=1-1">Women&#8217;s Encyclopedia of Natural Medicine: Alternative Therapies and Integrative Medicine for Total Health and Wellness</a> McGraw-Hill; 2 edition (Sep 20 2007)</p>
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<p>11. Ayhan Abaci, MD; Ihsan Esen, MD; Tolga Unuvar, MD; Nur Arslan, MD; Ece Bober, MD. Two Cases Presenting With Pubertal Delay and Diagnosed as Celiac Disease. Clinical pediatrics. <a title="http://cpj.sagepub.com/cgi/content/abstract/47/6/607" href="http://cpj.sagepub.com/cgi/content/abstract/47/6/607">http://cpj.sagepub.com/cgi/content/abstract/47/6/607</a></p>
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<p>12. Gianni Bona, Daniela Marinello, Giuseppina Oderda. Mechanisms of Abnormal Puberty in Coeliac Disease. <i>Horm Res</i> 2002;57:63-65.</p>
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<p>13. Coeliac disease and birth defects in offspring. (Letters to the editor) <i>Gut</i> 2001;49:738; doi:10.1136/gut.49.5.738 </p>
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<p>14. Aubrey J. Katz M.B., B.Ch., F.C.P.<sup>1</sup>, Z. Myron Falchuk M.D.<sup>1</sup>, and Harry Shwachman M.D.<sup>1</sup>The Coexistence of Cystic Fibrosis and Celiac Disease. PEDIATRICS Vol. 57 No. 5 May 1976, pp. 715-721. </p>
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<p>15. Malena Cohen-Cymberknoh<sup>1</sup>, Michael Wilschanski<sup>2</sup> Concomitant cystic fibrosis and coeliac disease: reminder of an important clinical lesson. <i>BMJ Case Reports</i> 2009 [doi:10.1136/bcr.07.2008.0578].&#160; Copyright © 2009 by the BMJ Publishing Group Ltd.</p>
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<p>16. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Venuta%20A%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Venuta A</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Bertolani%20P%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Bertolani P</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Casarini%20R%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Casarini R</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Ferrari%20F%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Ferrari F</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Guaraldi%20N%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Guaraldi N</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Garetti%20E%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Garetti E</b></a>. Coexistence of cystic fibrosis and celiac disease. Description of a clinical case and review of the literature. <a href="http://www.ncbi.nlm.nih.gov/">Pediatr Med Chir.</a> 1999 Sep-Oct;21(5 Suppl):223-6.</p>
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<p>17. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Sharma%20KA%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Sharma KA</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Kumar%20A%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Kumar A</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Kumar%20N%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Kumar N</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Aggarwal%20S%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Aggarwal S</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Prasad%20S%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Prasad S</b></a>. Celiac disease in intrauterine growth restriction. <a href="http://www.ncbi.nlm.nih.gov/">Int J Gynaecol Obstet.</a> 2007 Jul;98(1):57-9. </p>
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<p>18. A.Gasbarrini, E.Torre, C.Trivellini, S.De Carolis, A.Caruso, G.Gasbarrini. Recurrent spontaneous abortion and intrauterine fetal growth retardation as symptoms of coeliac disease. <em>The Lancet</em>, Volume 356, Issue 9227, Pages 399-400.</p>
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<p>19. Rami Eliakim<sup>a</sup>, David M. Sherer<sup>b</sup> Celiac Disease: Fertility and Pregnancy. <i>Gynecol Obstet Invest</i> 2001;51:3-7.</p>
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<p>20. Porpora, Maria Grazia MD; Picarelli, Antonio MD; Porta, Romana Prosperi MD; Di Tola, Marco BSc; D&#8217;Elia, Claudia MD; Cosmi, Ermelando Vinicio MD, PhD.&#160; Celiac Disease as a Cause of Chronic Pelvic Pain, Dysmenorrhea, and Deep Dyspareunia. Obstetrics &amp; Gynecology: May 2002 &#8211; Volume 99 &#8211; Issue 5, Part 2 &#8211; p 937-939.</p>
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<p>40. Adams Scott. Impotency and Celiac Disease. <a href="http://www.celiac.com">www.celiac.com</a>&#160; <b><a href="http://tinyurl.com/yeawdrv">http://tinyurl.com/yeawdrv</a></b></p>
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<p>41<strong>. </strong>Gibney MJ, Marinos E, Olle L, Dowsett J. Clinical Nutrition. Blackwell Publishing 2005.</p>
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<p>43. S. E. Ferguson<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B6WN2-457D05B-J&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1030112612&amp;_rerunOrigin=scholar.google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=f937b073506a79c3683a3c80123890c7#a1"><sup>a</sup></a>, G. N. Smith<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B6WN2-457D05B-J&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1030112612&amp;_rerunOrigin=scholar.google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=f937b073506a79c3683a3c80123890c7#a2"><sup>b</sup></a> and M. C. Walker<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B6WN2-457D05B-J&amp;_user=10&amp;_rdoc=1&amp;_fmt=&amp;_orig=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_searchStrId=1030112612&amp;_rerunOrigin=scholar.google&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=f937b073506a79c3683a3c80123890c7#a1"><sup>a</sup></a> Maternal plasma homocysteine levels in women with preterm premature rupture of membranes. <a href="http://www.sciencedirect.com/science/journal/03069877"><b>Medical Hypotheses</b></a>&#160;<a href="http://www.sciencedirect.com/science?_ob=PublicationURL&amp;_tockey=%23TOC%236950%232001%23999439998%23286434%23FLP%23&amp;_cdi=6950&amp;_pubType=J&amp;view=c&amp;_auth=y&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=be6c569595dd5d91aa3a0816aee111cc">Volume 56, Issue 1</a>, January 2001, Pages 85-90. </p>
<p>44. Edward J. Massaro and John M. Rogers. Folate And Human Development. Humana Press; 1 edition (Mar 10 2002)</p>
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<p>45. Robert A. DiSilvestro. Handbook Of Minerals As Nutritional Supplements. CRC Press LLC, 2005.</p>
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<p>47. Namanjeet Ahluwalia<sup>*</sup> and Hélène Grandje. Nutrition, an Under-Recognized Factor in Bacterial Vaginosis. <a href="http://jn.nutrition.org/misc/terms.shtml">American Society for Nutrition</a> J. Nutr. 137:1997-1998, September 2007.</p>
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<p>54. Ron Hoggan. Medical Superstitions of the Twenty-First Century. <a href="http://www.celiac.com">www.celiac.com</a>&#160; <b><a href="http://tinyurl.com/bwvo9p">http://tinyurl.com/bwvo9p</a></b> </p>
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		<title>Part 5 Of 12 Part Series: Musculoskeletal (Rickets, Osteomalacia, Osteopenia, Osteoporosis, Arthritis, And Myopathies) Symptoms In Undiagnosed Celiac Disease</title>
		<link>http://celiacnurse.com/musculoskeletal-rickets-osteomalacia-osteopenia-osteoporosis-arthritis-and-myopathies-symptoms-in-undiagnosed-celiac-disease/</link>
		<comments>http://celiacnurse.com/musculoskeletal-rickets-osteomalacia-osteopenia-osteoporosis-arthritis-and-myopathies-symptoms-in-undiagnosed-celiac-disease/#comments</comments>
		<pubDate>Fri, 25 Sep 2009 01:14:32 +0000</pubDate>
		<dc:creator>Shelly</dc:creator>
				<category><![CDATA[12 Part Series: CD Symptoms]]></category>

		<guid isPermaLink="false">http://celiacnurse.com/musculoskeletal-rickets-osteomalacia-osteopenia-osteoporosis-arthritis-and-myopathies-symptoms-in-undiagnosed-celiac-disease/</guid>
		<description><![CDATA[This is the fifth in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, musculoskeletal symptoms will be discussed. In many with undiagnosed CD, the intestinal villi, responsible for absorbing nutrients, becomes damaged, creating a flattened mucosal surface (villous flattening) that is less [...]]]></description>
			<content:encoded><![CDATA[<p>This is the fifth in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, musculoskeletal symptoms will be discussed. In many with undiagnosed CD, the intestinal villi, responsible for absorbing nutrients, becomes damaged, creating a flattened mucosal surface (villous flattening) that is less able to absorb nutrients. Autoimmune reactions to ingested gluten cross-react with intestinal villi and create this damage. Various nutrient deficiencies can occur and this, along with inflammation and other autoimmune factors, can lead to various musculoskeletal symptoms (1,2,3,4).<br />
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</p>
<h3><strong>Rickets And Osteomalacia</strong></h3>
<p>CD autoimmune factors, associated inflammation and malabsorption of nutrients can start demineralizing sketetal bones in infancy or childhood (rickets) and this can continue into adulthood (osteomalacia). In some, the pathological demineralizing effects of CD may not be triggered until adulthood. The bone structure becomes soft, weak, and bendable loosing it’s rigidity. This can lead to disfiguring disabilities such as <strong>bow legs, pigeon chest, pelvic deformities, deformed skull, and spine deformities (ex. lordosis, scoliosis, and kyphosis</strong>) possibly decreasing mobility (1,2,3,7,8,9,10,12-16,79). Osteomalacia can coexist with arthritis and osteoporosis (79). The damaging life long effects can be permanent. A CD diagnosis and a gluten-free could be the perfect primary prevention for those with undiagnosed CD. The symptoms of CD can be so elusive that diagnosis is often delayed for years (1,2,3).</p>
<p>Symptoms of rickets in infancy and childhood may include <strong>bone pain or tenderness, muscle weakness, seizures, failure to thrive, dental deformities and cavities, delayed or impaired growth, short stature, bone fractures, skeletal deformities (ex. bowed legs, pigeon chest, pelvic deformities, deformed skull, and/or curvature of the spine that is abnormal) muscle cramps/spasms, tetany, numbness, tingling, abnormal heart rhythms, difficulty crawling and sitting, and delayed walking</strong> (7,10,73,79). Early symptoms of osteomalacia in adulthood may initially be absent. During this initial phase, it may be diagnosed if apparent on a x-ray or other tests. As osteomalacia becomes chronic, symptoms may include <strong>muscle weakness, muscle cramps/spasms, tetany, seizures, numbness, tingling, abnormal heart rhythms, bone pain or tenderness, spine deformities, skeletal deformities, fractures, rachitic rosary, dental caries, reduced mobility, a change in gait, and a waddling gait</strong> (8,73,79). </p>
<h3><strong>Osteopenia And </strong><strong>Osteoporosis</strong></h3>
<p>A number of studies have identified an association between osteoporosis and CD. Demineralization of the bones in CD may result from an immunological process that is destructive to bones combined with malabsorption of important nutrients, primarily vitamin D, calcium, magnesium, and phosporus. Decreased mineral content of the bone is evident in osteopenia and chronic osteopenia can lead to weak, brittle bones (fragile and porous) evident in osteoporosis. This increases the <strong>risk for fractures</strong> (1,2,5,6,17-23,47,79). </p>
<p><strong>Symptoms</strong> may be absent initially. As the disease progresses, symptoms may include <strong>tetany, muscle weakness, muscle cramps/spasms, numbness, tingling, palpitations (irregular heart rhythms), convulsions, loss of height, low back or neck pain, stooped posture, bone pain or tenderness, collapsed vertebrae or other fractures</strong> (1,9,23-27,79). Testing for celiac disease and gluten antibodies is recommended for all individuals with osteoporosis, even in the absence of bowel symptoms&#160; (5,52).</p>
<p>Usually, supplementation with calcium and vitamin D along with a strict gluten-free diet and bone building exercises can result in remineralization of the skeletal bones (1,23-27). Your physician may prescribe additional treatment such as medications (ex. actonel, fosamax) to promote bone remineralization. However, Dr. Green, in his book “Celiac Disease”, recommends waiting until the intestine has healed to initiate this type of medication. Apparently, these medications might reduce blood calcium to a dangerous level potentially causing serious side effects such as arrhythmias, seizures, and muscular symptoms if given while the small intestine is still damaged. This is due to the bowel’s reduced ability to absorb calcium during the healing phase combined with the medications protective effect on bone breakdown. Usually, the blood can borrow the calcium from the bone to maintain homeostasis in the blood serum. The medication can prevent this from happening and this combined with the bowel’s reduced ability to absorb calcium can cause a deficiency in the blood. Diagnosed Celiacs with no intestinal involvement may not have this problem (1). </p>
<p><em>When I was diagnosed with CD, I was told I had osteopenia (borderline osteoporosis) and the bone density of my spine was comparable to a 76 year old (I was 38). I did some research, and then decided to choose the medication-free approach. My bone density returned to normal within 2 years on a strict gluten-free, nutrient dense diet, bone building exercises, and vitamin plus mineral supplements. I met with a Registered Dietician and my MD monitored me closely (with the Gastroenterologist’s guidance) during this time. While undiagnosed, I also experienced muscle weakness, muscle cramps/spasms in my calves and feet, numbness, tingling, palpitations, and tenderness in my lower back and my neck. I was informed about 10 years ago that I had a healed fracture on one of my ribs. I skydived, rock climbed, and white water kayaked frequently prior to having children and assumed this may have happened during this time. I’m surprised I didn’t have more fractures given that my bone density was likely poor for many years prior to diagnosis. My mother was diagnosed with osteoporosis and has CD. My daughter, also with CD, had occasional leg cramps. My mother and daughter did not have bowel symptoms prior to diagnosis.</em></p>
<h3><strong>Nutrient Deficiencies Contributing To Rickets, Osteomalcia, Osteopenia, And Osteoporosis&#160; </strong></h3>
<p>Nutrient deficiencies (common in CD) that may contribute to skeletal symptoms include vitamins <strong>A, D, E, K</strong>, and <strong>calcium, magnesium</strong>, <strong>phosphorus, protein, fatty acids, manganese, molybdenum, copper, boron, flouride, and zinc</strong> (1,5,6,70-74,79). </p>
<h3><strong>Arthritis And Joint Pain</strong></h3>
<p>Various types of arthritis, such as <strong>rheumatoid arthritis, osteoarthritis, polyarthritis, monoarthritis, sarcoilitis</strong>, <strong>ankylosing spondylitis</strong> and <strong>psoriatric arthritis</strong>, have been associated with gluten sensitivity and CD. In arthritis, joint inflammation can lead to destructive tissue damage within and around the joints. In addition to this, some types of arthritis can also damage other areas of the body (ex. skin and organs) (2,3,5,6,28-37,50,51,55). Arthritis symptoms can include <strong>swelling, pain, stiffness, redness, tenderness, and warmth in the affected areas,</strong> <strong>loss of function in affected area, and disfigured joint areas </strong>(50,56).</p>
<p>Over 100 types of arthritis have been identified (50). More research needs to be done to look at the effect gluten and other food sensitivities have on various types of arthritis. The effects of chronic arthritis symptoms can be debilitating affecting an individual’s psychological (decreased quality of life) and physical health. The risks associated with changing one’s diet is minimal (need to ensure foods are nutrient dense and that you consume all essential nutrients) compared with the possible risks associated with the side effects of medication (5,6). Many have found relief from arthritis symptoms by identifying sensitivities or allergies, then avoiding those foods (5,31,36,53,54,57,58). Dr. Gislason said that <strong>dairy, eggs, wheat, gluten, chocolate, potatoes, beef, pork, tomatoes, citrus fruits, almonds, wine</strong>, and certain medications can cause arthritic symptoms (58). A celiac screen and a consultation with an allergist and/or naturopathic doctor may be helpful. There are a variety of tests that are useful for identifying allergies and sensitivities. Some individuals use the core or elimination diet to do this. </p>
<p><strong>Nutrient deficiencies</strong> (common in CD) that may contribute to arthritis symptoms include vitamins <strong>A, D, C, E, K</strong>, <strong>niacin, pantothenic acid, pyridoxine, and protein, fatty acids, calcium, magnesium, iron, selenium, manganese, boron, copper, and zinc (70-74).</strong></p>
<p><em>Prior to diagnosis, I experienced pain and stiffness in both knees, my shoulder, my wrist, and my hip. Once diagnosed and gluten-free, the pain and stiffness disappeared only to return occasionally. I removed dairy from my diet and the pain and stiffness only returns when I eat dairy. Recently, I had a piece of gluten-free cheesecake (as an experiment) and I woke up the next morning with very stiff and sore fingers that were difficult to move. My arthritic symptoms appear to be linked to celiac disease and a dairy sensitivity. I now eat gluten-free and diary-free. </em></p>
<h3><strong>Muscular Symptoms</strong></h3>
<p>Muscle symptoms may result from immunological reactions affecting the nerves or muscle tissue, a compromised blood supply to the muscles, intramuscular bleeding, and/or nutrient deficiencies. <strong>Muscular symptoms can include cramps, stiffness, spasms, weakness, aching, pain, fatigue, swallowing difficulties (dysphagia), droopy eyelids, difficulty moving eyes, eye paralysis, limb weakness, weakness after exertion, tetany, decreased mobility, difficulty climbing stairs, difficulty breathing, myocarditis, decreased muscle mass, difficulty lifting objects or doing activities of daily living (3,12,13,38-46,48,49,56,59-63,65-70).</strong> If CD tests are negative, keep in mind that muscular symptoms can occur with gluten sensitivities, food allergies or sensitivities in the absence of CD. Gluten and dairy were specifically mentioned as possible antigens to try eliminating from one’s diet (48,49,58,76). An allergist or naturopathic doctor may be helpful to identify offending foods.</p>
<p>Myopathy involves a disease process that leads to dysfunctional muscle fibres. Various myopathies have been associated with CD and gluten sensitivity including <strong>dermatomyositis, polymyositis, inclusion body myositis, rhabdomyolysis, ocular myopathy, muscular dystrophy, neutrophillic myositis, muscular hypotonia of the infant or child, proximal myopathy and generalized myopathy</strong> (12,13,38-46,48,49,59-63,65-70). Intramuscular hemorrhage was also identified in one case study and this symptom was due to a vitamin K deficiency (75).</p>
<p><strong>Nutrient deficiencies</strong> (common in CD) that may contribute to muscular symptoms include vitamins <strong>A, D, E, K, niacin, thiamine, pantothenic</strong> <strong>acid, pyridoxine, <strong>cobalamin, </strong>protein, fat, carbohydrates, calcium, magnesium, phosporus, potassium, iodine, iron, and copper</strong> (70-74).&#160;&#160; </p>
<p><em>I experienced muscle cramps, stiffness, weakness, aching, fatigue, and had weakness after exertion. There were times I felt so weak that I had to sit or lie down for awhile. My daughter and mother both had muscle cramps. </em></p>
<h3><strong>Other Influencing Factors</strong></h3>
<p>Other factors that may contribute to musculoskeletal symptoms include a poor diet, past stomach or intestinal surgery, decreased sun exposure, gender, age, obesity, type of work, pregnancy, lactation, exclusively breast feeding without infant vitamin D supplements (inquire with MD), certain medications, dark skin (more difficult to produce vitamin D), low body weight, smoking, family history, early menopause, alcoholism, increased homocysteine levels, chronic bedrest, lack of exercise, and the presence of diarrhea and vomiting. The presence of other conditions such as renal failure, renal tubular acidosis, tumor-induced osteomalacia, cancer, acquired disorders of vitamin D metabolism, liver disease, Crohn’s disease, hypoparathyroidism, hyperthyroidism, compensatory secondary hyperparathyroidism, Cushing Syndrome, Paget’s disease,&#160; scleroderma, lupus, and sjögren’s syndrome may contribute to the symptoms as well (1,5,7,8,9,50,80).</p>
<h3><strong>Do You Have Any Of The Above Symptoms?</strong></h3>
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<p><strong>CD can be present in children that are growing normally so normal growth rate should not be a factor that excludes the possibility of CD (11). Many individuals with undiagnosed CD will have no bowel symptoms (25,26,52,60). Weight loss may or may not occur, and is dependent on the amount of the intestine that is damaged (25,60). Therefore, the symptoms in this post could occur in the absence of stunted growth, weight loss, or bowel symptoms.</strong></p>
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<p>The presence of musculoskeletal symptoms as discussed in this post, indicates that you should <strong>talk to your MD about</strong> <strong>tests for CD and tests to rule out other possible causes of your symptoms.</strong> Testing for CD is important because undiagnosed CD increases the risk of developing other autoimmune diseases, lymphomas (skin, brain, lymph nodes, intestine), cancers (thyroid, esophageal, mouth, tongue, pharynx, tonsil, and small intestine), allergies, complications from malabsorption issues, possible decreased immune response to other illnesses (1,2,77,78), and many other health complications that will be discussed in the posts about CD symptoms. It is my hope that if you have musculoskeletal symptoms you can print out this post complete with medical references to take with you to the MD when you request a CD test. Highlight or underline the sections that apply to your symptoms. I’ll be posting a simplified summary and checklist in the 12th post.</p>
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<p>It is possible to have a gluten sensitivity even if you test negative for CD. It is also possible that some of your symptoms could be due to a food allergy/sensitivity or other disease process.&#160; Allergy testing, and/or an elimination diet may help you to identify the offending food (5,6,31,36,48,49,53,54,57,58,76). Other tests can help rule out other diseases. I encourage everyone to have their symptoms thoroughly investigated by their MD and specialists before implementing a therapeutic diet. Keep your MD informed about any dietary changes you are making and also the results. Of course, I would love to hear your story as well.</p>
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<p><strong>I recommend waiting until CD testing is complete before initiating a gluten-free diet because it may create a false negative. Discuss this with your MD or specialist. <strong>USE CAUTION WITH SUPPLEMENTS. </strong>Toxicities can occur with over supplementation and this can lead to permanent damage. Consult your MD, Registered Dietitian, or other medical specialists involved in your care to determine which nutrients should be supplemented and to identify appropriate dosages for you.</strong> <strong>Review your symptoms and everything in this post with a Medical Doctor</strong> <strong>and your specialists before you make any changes</strong>. <strong>Your MD knows your medical history and the treatments that are appropriate for you.</strong></p>
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<p><strong>D</strong><strong>iagnosed Celiacs and people with food allergies/sensitivities</strong>, please comment about your symptoms&#160; and experiences at the end of each post. This will help other readers to see how the sometimes illusive symptoms of CD or food sensitivities can affect each of us.&#160; We are all unique!</p>
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<h3><strong>References</strong></h3>
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<p><cite>1. <strong>Excellent Book:</strong> Green PHR, Jones, R. Celiac Disease A Hidden Epidemic. Collins, Harper Collins Publishers, 2006 <b>http://tinyurl.com/ljeqjc</b></cite></p>
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<p><cite></cite><cite>2. </cite>Pruessner Harold T, MD. Detecting Celiac Disease In Your Patients. American Family Physician. March 1st, 1998.</p>
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<p>3. Feldman Mark, MD, Friedman Lawrence S, MD, Sleisenger, Marvin H, MD, Gastrointestinal and Liver Disease Pathophysiology/Diagnosis/Management 7th Edition, Volume11, 2002,Saunders</p>
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<p>4. Barrett KE. Gastrointestinal Physiology. Lange Medical Books/McGraw-Hill 2006.</p>
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<p>5. <strong>Excellent Book:</strong> Lieberman Shari PhD,CNC, FACN, with Linda Segall. The Gluten Connection. How Gluten Sensitivity May Be Sabotaging Your Health. Rodale Inc., 2007. <b>http://tinyurl.com/nwsc79</b></p>
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<p>6. <strong>Excellent Book:</strong> James Braly, MD., Ron Hoggan, MA. Dangerous Grains. Penguin Group, Inc., 2002. <b><a href="http://tinyurl.com/knswhn">http://tinyurl.com/knswhn</a></b></p>
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<p><strong>7. Rickets <a title="http://www.nlm.nih.gov/medlineplus/ency/article/000344.htm" href="http://www.nlm.nih.gov/medlineplus/ency/article/000344.htm">http://www.nlm.nih.gov/medlineplus/ency/article/000344.htm</a></strong></p>
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<p><strong>8. Osteomalacia <a title="http://www.nlm.nih.gov/medlineplus/ency/article/000376.htm" href="http://www.nlm.nih.gov/medlineplus/ency/article/000376.htm">http://www.nlm.nih.gov/medlineplus/ency/article/000376.htm</a></strong></p>
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<p>9. Osteoporosis <a title="http://www.nlm.nih.gov/medlineplus/ency/article/000360.htm" href="http://www.nlm.nih.gov/medlineplus/ency/article/000360.htm">http://www.nlm.nih.gov/medlineplus/ency/article/000360.htm</a></p>
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<p>10. Cimaz R, , Bazzi P, Prelle A. Myopathy associated with rickets and celiac disease. Acta Paediatr 2000 Apr;89(4):496-7.</p>
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<p>11. Lejarraga H, et el. Normal Growth Velocity Before Diagnosis Of Celiac Disease. J Pediatr Gastrenterol Nutr 2000;30:552-556.</p>
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<p>12. Mehmet D. Demirag<sup>a</sup>, Berna Goker<sup>a</sup>, Seminur Haznedaroglu<sup>a</sup>, Mehmet A. Ozturk<sup>a</sup>, Tarkan Karakan<sup>b</sup>, Reha Kuruoglu<sup>c. </sup>Osteomalacic Myopathy Associated with Coexisting Coeliac Disease and Primary Biliary Cirrhosis. <i>Med Princ Pract</i> 2008;17:425-428</p>
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<p>13. Costantine Albany, MD, Zhanna Servetnyk, MD, PhD. Disabling Osteomalacia And Myopathy As The Only Presenting Features Of Celiac Disease: A Case Report. Department of Medicine, St. Luke’s Roosevelt Hospital Centre, Columbia University College of Physicians And Surgeons.</p>
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<p>14. Harzy T, et el. An Unusual Case of Osteomalacia As The Presenting Feature Of Coeliac Disease. Rheumatol Int, 2005. 26(1):p.90-91.</p>
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<p>15. Basu RA,et el. Coeliac Disease Can Still present With Osteomalacia! Rheumatology (Oxford), 2000. 39(3):p335-336.</p>
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<p>17. Meyer D, Stavropoulos S, Diamond B, Shane E, Green PHR. Osteoporosis In A North American Adult Population With Celiac Disease. Am J Gastroenterol 2001, 96:112-119.</p>
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<p>18. Vazquez H, Mazure R, Gonzalez D, Flores D, Pedreira S, Niveloni S, Smecuol E, Maurino E, Bai JC. Risk Of Fractures In Celiac Disease Patients: A Cross-Sectional, Case Control Study. Am J Gastroenterol 2000;95(1):183-189.</p>
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<p>19. Ferretti J, Mazure R, Tanoue P, Marino A, Cointry G, Vazquez H, Niveloni S, Pedreira S, Maurino E, Zanchetta J, Bai JC. Analysis Of The Structure And Strength Of Bones In Celiac Disease Patients. Am J Gastroenterol 2003;98(2):382-90.</p>
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<p>20. Kemppainen T. Osteoporosis in adult patients with celiac disease. <em>Bone</em>, Volume 24, Issue 3, Pages 249-255.</p>
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<p>21. Endonurse. Screening Patients with Osteoporosis for Celiac Disease Appears Worthwhile. 03/01/2005. <a title="http://www.endonurse.com/hotnews/53h1162048334.html" href="http://www.endonurse.com/hotnews/53h1162048334.html">http://www.endonurse.com/hotnews/53h1162048334.html</a> Reference in article: February 28 issue of <i>Archives of Internal Medicine</i>, one of the JAMA/Archives journals.</p>
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<p>22. Patients With Osteoporosis Should Be Screened For Celiac Disease, Study Suggests. ScienceDaily (Mar. 16, 2005) — St. Louis, Feb. 28, 2005. <a title="http://www.sciencedaily.com/releases/2005/03/050308131921.htm" href="http://www.sciencedaily.com/releases/2005/03/050308131921.htm">http://www.sciencedaily.com/releases/2005/03/050308131921.htm</a></p>
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<p>24. David A Nelson, JR., MD., MS., University of Arkanas for Medical Sciences, Little Rock, Arkansas. Gluten-Sensitive Enteropathy (Celiac Disease): More Common Than You Think. American Family Physician, December 15, 2002.</p>
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<p>25. Feldman Mark, MD, Friedman Lawrence S, MD, Sleisenger, Marvin H, MD, Gastrointestinal and Liver Disease Pathophysiology/Diagnosis/Management 7th Edition, Volume11, 2002,Saunders</p>
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<p>26. Kagnoff MF. AGA Institute Medical Position Statement on the Diagnosis and Management of CD. Gastroenterology, Official Journal of the American Gastroenterological Association (AGA). November 2006.</p>
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<p>27. Unsure of Author, The American Journal of Managed Care.2003;9:825-831.</p>
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<p>29. Lubrano et el. The Arthritis of Celiac Disease: Prevalence And Pattern In 200 Adult Patients. British Journal of Rheumatology. 1996;35:1314-8.</p>
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<p>30. Bourne JT, Kumar P, Huskisson EC, Mageed R, Unsworth DJ, Wojtulewski JA. Arthritis And Celiac disease. Ann Rheum Dis 1985, September;44(9):592-598.</p>
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<p>31. Adams Jefferson. Studies Show High Instance of Rheumatoid Arthritis And Osteoporosis In Patients With Celiac Disease. <a href="http://www.celiac.com">www.celiac.com</a> </p>
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<p>32. Collin P, Korpela M, Hallstrom O, et el. Rheumatic Complaints As A Presenting Symptom In Patients With Celiac Disease. Scan J Rheumatol 1992;21:20-3.</p>
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<p>33. Usai P. Adult Celiac disease is Frequently Associated With Sarcoilitis. Dig Dis Sci 1995;40:1906-8.</p>
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<p>34. Bagnato GF, Quattrocchi E, Gulli S et el. Unusual Polyarthritis As A Unique Clinical Manifestation Of Celiac Disease. Rheumatol Int 2000;20:29-30.</p>
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<p>35. Borg AA, Dawes PT, Swan CH, Hathersall TE. Persistant Monoarthritis And Occult Celiac Disease. Postgrad Med j 1994;70:51-53.</p>
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<p>36. Adams Scott. Arthritis And Celiac Disease. <a href="http://www.celiac.com">www.celiac.com</a></p>
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<p>37. U. Lindqvist<sup>1</sup><a name="RFN1"></a><sup>,</sup>, Å. Rudsander<sup>1</sup><sup>,2</sup>, Å. Boström<sup>2</sup>, B. Nilsson<sup>3</sup> and G. Michaëlsson<sup>2. </sup>IgA antibodies to gliadin and coeliac disease in psoriatic arthritis. Rheumatology 2002; 41: 31-37.</p>
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<p>38. Sandyk R., MD, Brennan M.J.W., MB, BCh, PhD. Isolated Ocular Myopathy And Celiac Disease In Childhood. Neurology 1983;33:792. American Academy Of Neurology.</p>
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<p>39. Wong M, et el. Proximal Myopathy And Bone Pain As The Presenting Features Of Coeliac Disease. Ann Rheum Dis, 2002, 61(1):p87-8.</p>
<p>40. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Kleopa%20KA%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus">Kleopa KA</a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Kyriacou%20K%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus">Kyriacou K</a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Zamba-Papanicolaou%20E%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus">Zamba-Papanicolaou E</a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Kyriakides%20T%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus">Kyriakides T</a>. Reversible inflammatory and vacuolar myopathy with vitamin E deficiency in celiac disease. <a href="http://www.ncbi.nlm.nih.gov/">Muscle Nerve.</a> 2005 Feb;31(2):260-5.</p>
<p>41. Possible Relationship Between Myopathies And Celiac Disease. ScienceDaily (Feb. 24, 2007) </p>
<p>42. Albert Selva-O&#8217;Callaghan, MD, PhD<sup> 1 *</sup>, Francesc Casellas, MD, PhD<sup> 2</sup>, Ines de Torres, MD, PhD<sup> 3</sup>, Eduard Palou, MD, PhD<sup> 4</sup>, Josep M. Grau-Junyent, MD, PhD<sup> 5</sup>, Miquel Vilardell-Tarrés, MD, PhD<sup> 1 </sup><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&amp;cmd=Retrieve&amp;dopt=AbstractPlus&amp;list_uids=16967485&amp;itool=pubmed_DocSum">Celiac disease and antibodies associated with celiac disease in patients with inflammatory myopathy</a>. <a href="http://www3.interscience.wiley.com/journal/32891/home">Muscle &amp; Nerve</a>, <strong><a href="http://www3.interscience.wiley.com/journal/113518454/issue">Volume 35 Issue 1</a>, Pages 49 – 54.</strong><strong>Published Online: </strong>11 Sep 2006</p>
<p><strong>43.</strong> Erkan Kozanoglu<sup>1</sup>, Sibel Basaran<sup>1</sup> and M. Kamil Goncu<sup>1. </sup>Proximal myopathy as an unusual presenting feature of celiac disease. Journal <a href="http://www.springerlink.com/content/102818/?p=67bdc6efa0c94181851ab20c64bd6f62&amp;pi=0">Clinical Rheumatology</a>. Issue <a href="http://www.springerlink.com/content/j64057amj92v/?p=67bdc6efa0c94181851ab20c64bd6f62&amp;pi=0">Volume 24, Number 1 / February, 2005</a>. Pages 76-78</p>
<p>44. Vivek Jain<sup>1</sup>, Rajeshwar Reddy Angitii<sup>1</sup>, Surjit Singh<sup>1</sup>, Babu Ram Thapa<sup>2</sup> and Lata Kumar<sup>1&#160; </sup><sup>Proximal Muscle Weakness—An Unusual Presentation of Celiac Disease. Department of Pediatrics, Postgraduate Institute of Medical Education and Research PGIMER), Chandigarh, India </sup></p>
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<p>47. Canadian Celiac Association Health Survey (2007)&#160; <b><a href="http://tinyurl.com/n3fbj7">http://tinyurl.com/n3fbj7</a>&#160; </b>Also in Digestive Diseases And Sciences April 2007:52(4):1087-1095.</p>
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<p>48. Roubenoff R, Coleman Laura A. Nutrition And Rheumatic Disease. Humana Press, 2008.</p>
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<p>49. Selva-O’Callaghan A, et el. Celiac disease And Antibodies Associated With Celiac Disease In Patients With Inflammatory Myopathy. Muscle Nerve, 2006;volume 35, issue 1,page 49-54.</p>
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<p>50. WebMd <a href="http://www.webmd.com/osteoarthritis/guide/arthritis-basics">Arthritis Basics</a>&#160;<a title="http://www.webmd.com/osteoarthritis/guide/arthritis-basics" href="http://www.webmd.com/osteoarthritis/guide/arthritis-basics">http://www.webmd.com/osteoarthritis/guide/arthritis-basics</a></p>
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<p>51. Slot D, Locht H. Arthritis As Presenting Symptom In Silent Adult Celiac Disease. Scandinavian Journal Of Rheumatology. 2000;29:260-3</p>
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<p>52. Stenson W, et el. Increased Prevalence Of Celiac Disease And Need For Routine Screening Among Patients With Osteoporosis. Archives Of Internal Medicine February 28, 2005;165(4).</p>
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<p>53. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Panush%20RS%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Panush RS</b></a>. Possible role of food sensitivity in arthritis. <a href="http://www.ncbi.nlm.nih.gov/">Ann Allergy.</a> 1988 Dec;61(6 Pt 2):31-5.</p>
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<p>69. Iannone F<strong>,</strong> Lapadula G. Dermatomyositis and celiac disease association: a further case. <i>Clin Exp R</i><i>heumatol</i> 2001; 19: 757-758</p>
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<p>71. Chernoff Ronni. Geriatric Nutrition: The Health Professionals Handbook. Jones And Bartlett Publishers Inc. 3rd edition, 2006.</p>
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<p>72. Kamhi Ellen, Zampierson Eugene R. Arthritis: Reverse Underlying&#160; Causes Of Arthritis With Clinically Proven Alternative Therapies. Celestial Arts. 2nd Edition, 2006.</p>
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<p>73. Gibney MJ, Marinos E, Olle L, Dowsett J. Clinical Nutrition. Blackwell Publishing 2005.</p>
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<p>74. Gibney MJ, Vorster HH, Kok FJ. Introduction to Human Nutrition. Blackwell Publishing 2002.</p>
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<p>75. Carolyn S. Chen, MD,<sup><img alt="corresponding author" src="http://www.pubmedcentral.nih.gov/corehtml/pmc/pmcgifs/corrauth.gif" /></sup><sup>1</sup> Ethan U. Cumbler, MD,<sup>2</sup> and Andrzej T. Triebling, MD, PhD<sup>3</sup> Coagulopathy Due to Celiac Disease Presenting as Intramuscular Hemorrhage. J Gen Intern Med. 2007 November; 22(11): 1608–1612. </p>
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		<title>Part 4 Of 12 Part Series: Skin Rashes, Hair, And Nail Symptoms In Undiagnosed Celiac Disease</title>
		<link>http://celiacnurse.com/skin-rashes-hair-and-nail-symptoms-in-undiagnosed-celiac-disease/</link>
		<comments>http://celiacnurse.com/skin-rashes-hair-and-nail-symptoms-in-undiagnosed-celiac-disease/#comments</comments>
		<pubDate>Fri, 18 Sep 2009 18:08:17 +0000</pubDate>
		<dc:creator>Shelly</dc:creator>
				<category><![CDATA[12 Part Series: CD Symptoms]]></category>

		<guid isPermaLink="false">http://celiacnurse.com/skin-rashes-hair-and-nail-symptoms-in-undiagnosed-celiac-disease/</guid>
		<description><![CDATA[This is the fourth in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, skin rashes, hair, and nail symptoms will be discussed. In many with undiagnosed CD, the intestinal villi, responsible for absorbing nutrients, becomes damaged, creating a flattened mucosal surface (villous [...]]]></description>
			<content:encoded><![CDATA[</p>
<dt>
<p>This is the fourth in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, skin rashes, hair, and nail symptoms will be discussed. In many with undiagnosed CD, the intestinal villi, responsible for absorbing nutrients, becomes damaged, creating a flattened mucosal surface (villous flattening) that is less able to absorb nutrients. Autoimmune reactions to ingested gluten cross-react with intestinal villi and create this damage. Various nutrient deficiencies can occur and this, along with inflammation and other autoimmune factors, can lead to various skin rashes, hair, and nail symptoms (1,2,3,4).&#160;<br />
<span id="more-102"></span>
</p>
<h3><strong>Skin Rashes And Other Skin Symptoms</strong></h3>
</dt>
<dt>
<h4><strong>Dermatitis&#160; Herpetiformis (Duhring’s Disease)</strong></h4>
</dt>
<dt>
<p>Dermatitis Herpetiformis (DH) occurs when autoimmune reactions lead to a skin rash. Unfortunately, this form of CD is often misdiagnosed as other various skin disorders and conditions (1). An individual with DH may be misdiagnosed with&#160; psoriasis, poison ivy, pustular psoriasis, shingles, scabies, acne, acne rosea, hives, unexplained dermatitis herpes, recurrent mites, mosquito bites, flea bites, eczema and many other possible diagnosis that will be listed below (1,5,6). Symptoms include a blistering (papulovesicular eruptions) or scabbed rash that is very itchy. As well, the rash can have pimple type lesions or look similar to psoriasis with raised red patches of skin. In children, the rash may only present as purpura on the palms of their hands (in isolation or in addition to other symptoms). Usually the rash occurs bilaterally on the body and is commonly found on the buttocks, back, elbows, forearms, back of knees, scalp and on the face. Clinically, the rash can present anywhere on the body (1,5,6,7).</p>
</dt>
<dt>
<p>In the book “Dangerous Grains” it mentioned that there are dermatologists who continue to prescribe medication for Dermatitis Herpetiformis without prescribing a strict gluten-free diet. Unfortunately, these patients may continue to have a high risk of associated cancers, other autoimmune damage or malabsorption issues (even without bowel symptoms) with this approach (6). <em>One Recreational Therapist that I worked with was diagnosed with DH and put on dapsone without being told about a gluten-free diet. The dermatologist did ask her if she had any bowel symptoms. She said no. Further tests were not completed and a gluten-free diet was not mentioned. Unfortunately, she suffered with side effects from the medication for 2 years with this approach. Following a discussion with me on a lunch break, she saw her MD, a gastroenterologist, and her dermatologist. She started a gluten-free diet and was able to discontinue the dapsone following a discussion with her doctor. Now, she is the picture of health, living rash and drug free.</em> Dr. Peter Green, in his book, “Celiac disease” said, “If you have a positive diagnosis of dermatitis herpetiformis, you have celiac disease. And you must adhere to a gluten-free diet no matter how “normal” your intestine may appear.” (1)</p>
</dt>
<dt>
<p>Dr. Green also identified that the normal blood tests (endomysial antibodies and antitissue transglutaminase) for celiac disease might be negative in DH since they tend to correspond with the severity of intestinal damage in CD, not the severity of skin damage. Therefore, absence of intestinal damage could lead to negative CD blood tests. Dr. Green also identified that the unaffected skin beside (within millimeters) the lesion should be biopsied, not the lesion itself. Apparently, the inflammation in the lesion itself may make it difficult to see (in immunological staining) the initial immune factors responsible for DH. A skin biopsy that is positive for DH indicates that a strict gluten-free diet should be started, even with a negative intestinal biopsy (1). If the skin biopsy and intestinal biopsy are negative, but the rash appears to occur after gluten consumption (can be up to many days), then the biopsies should be repeated and and gluten sensitivities should be investigated. Rashes can result from food allergies or a gluten sensitivity in the absence of CD or DH (1,5,6,77,85).</p>
</dt>
<dt>
<p><strong>Pictures of DH may be seen at <b><a href="http://tinyurl.com/qsge4v">http://tinyurl.com/qsge4v</a></b>, <b><a href="http://tinyurl.com/l3s2fa">http://tinyurl.com/l3s2fa</a></b>, <b><a href="http://tinyurl.com/n3x4ls">http://tinyurl.com/n3x4ls</a></b>, or <b><a href="http://tinyurl.com/n9fo8x">http://tinyurl.com/n9fo8x</a></b>. </strong></p>
</dt>
<dt>
<p>&#160;</p>
</dt>
<dt>
<h4><strong>List Of Other Skin Rashes/Conditions Associated With Celiac Disease And Gluten Intolerance</strong></h4>
<ul>
<li>
<p>Cutaneous vasculitis (7,8-11)</p>
</li>
<li>
<p>Hereditary Angioneurotic Edema (7,12-15)</p>
</li>
<li>
<p>Urticaria (7,15-20,85)</p>
</li>
<li>
<p>Linear IgA bullous dermatosis (7,21-25)</p>
</li>
<li>
<p>Erythema nodosum (7,26-28)</p>
</li>
<li>
<p>Necrolytic migratory erythema (7,29-32,85)</p>
</li>
<li>
<p>Erythema elevatum diutinum (7,33-35)</p>
</li>
<li>
<p>Psoriasis (7,36-44,78,85)</p>
</li>
<li>
<p>Vitiligo (7,45-48,78)</p>
</li>
<li>
<p>Behçet’s disease (7,49)</p>
</li>
<li>
<p>Dermatomyositis (7,50-54,85)</p>
</li>
<li>
<p>Porphyria&#160; (7,55-57)</p>
</li>
<li>
<p>Ichthyosiform dermatoses (7,58)</p>
</li>
<li>
<p>Pellagra (7,59)</p>
</li>
<li>
<p>Generalized acquired cutis laxa (7,60,61,85)</p>
</li>
<li>
<p>Atypical mole syndrome and cogenital giant naevus (7,62-66)</p>
</li>
<li>
<p>Prurigo nodularis (hyde’s prurigo) (71,85)</p>
</li>
<li>
<p>Pityriasis rubra pilaris (72,85)</p>
</li>
<li>
<p>Erythroderma (85)</p>
</li>
<li>
<p>Acne (73)</p>
</li>
<li>
<p>Acquired hypertrichosis lanuginosa (67)</p>
</li>
<li>
<p>Ichthyosis (74,85)</p>
</li>
<li>
<p>Transverse Leukonychia (85)</p>
</li>
<li>
<p>Follicular Hyperkeratosis (78)</p>
</li>
<li>
<p>Scleroderma (80)</p>
</li>
<li>
<p>Sarcoidosis (28,78)</p>
</li>
<li>
<p>Oral Lichen Planus (68-70)</p>
</li>
<li>
<p>Bullous pemphigoid (85)</p>
</li>
<li>
<p>Angular Cheilitis, glossitis, ulcerative stomatitis, and aphthous ulcers (78,79,85)</p>
</li>
<li>
<p>Pale skin (from anemia) (78,79)</p>
</li>
<li>
<p>Dry and/or cracked skin from dehydration and malabsorption of nutrients (80,81)</p>
</li>
<li>
<p>Delayed wound healing (malabsorption of nutrients) (81,82)</p>
</li>
<li>
<p>Edema (swollen skin) (78,79)</p>
</li>
<li>
<p>Any itchy skin rashes (78)</p>
</li>
<li>
<p>Melanoma (75)</p>
</li>
<li>
<p>Dermatitis or acrodermatitis (78,79)</p>
</li>
<li>
<p>IgA Linear dermatosis (85)</p>
</li>
<li>
<p>Lupus erythematosus (85)</p>
</li>
<li>
<p>Lichen sclerosous (85)</p>
</li>
<li>
<p>Cutaneous amyloidosis (85)</p>
</li>
<li>
<p>Annular erythema (85)</p>
</li>
<li>
<p>Partial lipodystrophy (85)</p>
</li>
<li>
<p>Atopic dermatitis (85)</p>
</li>
<li>
<p>Palmoplantar pustulosis (85)</p>
</li>
<li>
<p>seborrheic dermatitis-from riboflavin deficiency (81,82)</p>
</li>
<li>
<p>Facial butterfly Rash-from niacin deficiency (81,82)</p>
</li>
<li>
<p>Increased skin pigmentation (79)</p>
</li>
<li>
<p>Spontaneous ecchymoses (78)</p>
</li>
<li>
<p>Bruised skin (79)</p>
</li>
<li>
<p>Purpura (79)</p>
</li>
<li>
<p>Petechia (78)</p>
</li>
<li>
<p>Bleeding under the skin (78)</p>
</li>
</ul>
<p><em>I experienced generalized dry skin and cracked peeling skin on the heels of my feet. My lips would crack at the corners and I had canker sores in my mouth. Occasionally, intensely itchy red raised areas would occur on various parts of my body and I would get little pimples on my scalp. A butterfly rash would develop over my nose about once a week for awhile, then it would disappear for a month or two (lupus tests were negative). I was always pale, and I did tend to bruise easily. My mother, also with CD, bruised easily, was pale, had dry skin (especially on her feet), and would develop an unusual blotchy rash around her neck area. My daughter, at age 4 (also with CD), had red itchy patches that would last a few hours, then disappear. My mother and daughter did not have bowel symptoms. My bowel symptoms started after the birth of my first child.</em></p>
</dt>
<dt>
<p><em>My middle child tested negative for CD. She had <strong>eczema </strong>of moderate severity, hyperactivity, lack of focus, occasional diarrhea, and abdominal discomfort. All medical tests ordered by the paediatric allergist were negative. An elimination diet revealed that she was sensitive to corn and corn derivatives (which are in most grocery store products). All symptoms resolved when I removed corn from her diet. All symptoms return with accidental ingestion of corn.</em></p>
</dt>
<dt>
<p>Nutrient deficiencies partially or fully contributing to the above skin symptoms may include vitamin A, B complex, C, K, essential fatty and amino acids, iron, zinc, biotin,copper, and manganese (78,79,81,82).</p>
</dt>
<dt>
<h3>Hair Symptoms</h3>
</dt>
<dt>
<p>Alopecia Areata (Patches of hair loss) has been associated with CD . In CD, it may be the result of an immunological attack and/or nutrient deficiencies (1,7,79,81,82,83,84,85). Alopecia can be the only presenting symptom in CD (7).</p>
</dt>
<dt>
<p>An individual with CD may have dry, thin, brittle, slow growing hair due to nutrient deficiencies. Hair might change color due to malabsorption issues with pantothenic acid or manganese deficiencies (81,82).</p>
</dt>
<dt>
<p><em>My mother and I had hair that grew slowly, was fine, and brittle</em>. </p>
</dt>
<dt>
<h3>Nail Symptoms</h3>
</dt>
<dt>
<p>Individuals with CD, may have nails that are dry, brittle, thin, malformed, and that break easily. This can be due to nutrient deficiencies or associated conditions. Nails may grow slowly and can also also have white bands, longitudinal striations, horizontal or vertical ridges, color changes, white spots, splinter hemorrhages, a deformed nail shape that is curved up or down (ex. spoon shaped with anemia), hang nails, or be clubbed. Muehrcke’s lines may indicate albumin levels are low. Beau’s lines can result from nutrient deficiencies disrupting nail growth, onycholysis can be associated with psoriasis or sarcoidosis, and the nails might be pitted (associated with psoriasis and alopecia). Telangiectasia may develop with underlying lupus, dermatomyositis, or scleroderma (86,87). Pictures and further description of these nail disorders can be found at <b><a href="http://tinyurl.com/lom4nt">http://tinyurl.com/lom4nt</a></b>.</p>
</dt>
<dt>
<p>Nutrients Deficiencies that can contribute to nail abnormalities can include, vitamin A, B complex, C, K, protein, calcium, iron, and zinc (86).</p>
</dt>
<dt>
<p><em>I had nail symptoms including dry, brittle, nails that broke easily. Hang nails were continuously present and my nails frequently had white spots. My mother had horizontal ridges on her dry, brittle nails.</em></p>
<h3><strong>Do You Have Any Of The Above Symptoms?</strong></h3>
</dt>
<dt>
<p><strong>Many individuals with undiagnosed CD will have no bowel symptoms (1,2,3,5,6,85). Weight loss may or may not occur, and is dependent on the amount of the intestine that is damaged (78). Therefore, the symptoms in this post could occur in the absence of weight loss or bowel symptoms.</strong></p>
</dt>
<dt>
<p>The presence of skin, hair, or nail symptoms as discussed in this post, indicates that you should <strong>talk to your MD about</strong> <strong>tests for CD and tests to rule out other possible causes of your symptoms.</strong> Testing for CD is important because undiagnosed CD increases the risk of developing other autoimmune diseases, lymphomas (skin, brain, lymph nodes, intestine), cancers (thyroid, esophageal, mouth, tongue, pharynx, tonsil, and small intestine), allergies, complications from malabsorption issues, possible decreased immune response to other illnesses (1,78,79,88,89), and many other health complications that will be discussed in the posts about CD symptoms. It is my hope that if you have any of these symptoms you can print out this post complete with medical references to take with you to the MD when you request a CD test. Highlight or underline the sections that apply to your symptoms. I’ll be posting a simplified summary and checklist in the 12th post.</p>
</dt>
<dt>
<p>It is possible to have a gluten sensitivity even if you test negative for CD. It is also possible that your symptoms could be due to a food allergy/sensitivity or other disease process.&#160; Allergy testing, and an elimination diet may help you to identify the offending food (5,6,77,85). Other tests can help rule out other diseases. I encourage everyone to have their symptoms thoroughly investigated by their MD and specialists before implementing a therapeutic diet. Keep your MD informed about any dietary changes you are making and also the results. Of course, I would love to hear your story as well.</p>
</dt>
<dt>
<p><strong>I recommend waiting until CD testing is complete before initiating a gluten-free diet because it may create a false negative. Discuss this with your MD or specialist. <strong>USE CAUTION WITH SUPPLEMENTS. </strong>Toxicities can occur with over supplementation and this can lead to permanent damage. Consult your MD, Registered Dietitian, or other medical specialists involved in your care to determine which nutrients should be supplemented and to identify appropriate dosages for you.</strong> <strong>Review your symptoms and everything in this post with a Medical Doctor</strong> <strong>and your specialists before you make any changes</strong>. <strong>Your MD knows your medical history and the treatments that are appropriate for you.</strong></p>
</dt>
<dt>
<p><strong>D</strong><strong>iagnosed Celiacs and people with food allergies/sensitivities</strong>, please comment about your symptoms&#160; and experiences at the end of each post. This will help other readers to see how the sometimes illusive symptoms of CD or food sensitivities can affect each of us.&#160; We are all unique!</p>
</dt>
<dt>
<h3><strong>References</strong></h3>
</dt>
<dt>
<p><cite>1. <strong>Excellent Book:</strong> Green PHR, Jones, R. Celiac Disease A Hidden Epidemic. Collins, Harper Collins Publishers, 2006 <b>http://tinyurl.com/ljeqjc</b></cite></p>
</dt>
<dt>
<p><cite></cite><cite>2. </cite>Pruessner Harold T, MD. Detecting Celiac Disease In Your Patients. American Family Physician. March 1st, 1998.</p>
</dt>
<dt>
<p>3. Feldman Mark, MD, Friedman Lawrence S, MD, Sleisenger, Marvin H, MD, Gastrointestinal and Liver Disease Pathophysiology/Diagnosis/Management 7th Edition, Volume11, 2002,Saunders</p>
</dt>
<dt>
<p>4. Barrett KE. Gastrointestinal Physiology. Lange Medical Books/McGraw-Hill 2006.</p>
</dt>
<dt>
<p>5. <strong>Excellent Book:</strong> Lieberman Shari PhD,CNC, FACN, with Linda Segall. The Gluten Connection. How Gluten Sensitivity May Be Sabotaging Your Health. Rodale Inc., 2007. <b>http://tinyurl.com/nwsc79</b></p>
</dt>
<dt>
<p>6. <strong>Excellent Book:</strong> James Braly, MD., Ron Hoggan, MA. Dangerous Grains. Penguin Group, Inc., 2002. <b>http://tinyurl.com/knswhn</b></p>
</dt>
<dt>
<p>7. Abenavoli L, Proietti I, Leggio L, Ferrulli A, Vonghia L, Capizzi R, Rotoli M, Amerio PL, Gasbarrini g, Addolorato G. Cutaneous Manifestations In Celiac disease. World Journal Of Gastroenterology. 2006 February 14;12(6):843-852.</p>
</dt>
<dt>
<p>8. Jones FA. The skin: a mirror of the gut. <i>Geriatrics</i> 1973; <b>28</b>: 75-81</p>
</dt>
<dt>
<p>9. Holdstock DJ<strong>,</strong> Oleesky S. Vasculitis in coeliac diseases. <i>Br Med J</i> 1970; <b>4</b>: 369</p>
</dt>
<dt>
<p>10. Meyers S, Dikman S, Spiera H, Schultz N, Janowitz HD. Cutaneous vasculitis complicating coeliac disease. <i>Gut</i> 1981; 22: 61-64</p>
</dt>
<dt>
<p>11. Similä S, Kokkonen J, Kallioinen M. Cutaneous Vasculitis As A Manifestation Of Celiac Disease. Acta Paediatrica Volume 71 Issue 6, Pages 1051-1054.</p>
</dt>
<dt>
<p>12. Brickman CM, Tsokos GC, Chused TM, Balow JE, Lawley TJ, Santaella M, Hammer CH, Linton GF, Frank MM. Immunoregulatory disorders associated with hereditary angioedema. II. Serologic and cellular abnormalities. <i>J Allergy Clin Immunol </i>1986; 77: 758-767</p>
</dt>
<dt>
<p>13. Farkas H, Gyeney L, Nemesanszky E, Kaldi G, Kukan F, Masszi I, Soos J, Bely M, Farkas E, Fust G, Varga L. Coincidence of hereditary angioedema (HAE) with Crohn&#8217;s disease. <i>Immunol Invest</i> 1999; 28: 43-53</p>
</dt>
<dt>
<p>14. Farkas H, Visy B, Fekete B, Karadi I, Kovacs JB, Kovacs IB, Kalmar L, Tordai A, Varga L. Association of celiac disease and hereditary angioneurotic edema. <i>Am J Gastroenterol</i> 2002; 97: 2682-2683</p>
</dt>
<dt>
<p>15. Hautekeete ML, DeClerck LS, Stevens WJ. Chronic urticaria associated with coeliac disease. <i>Lancet</i> 1987; <b>1</b>: 157</p>
</dt>
<dt>
<p>16. Gabrielli M, Candelli M, Cremonini F, Ojetti V, Santarelli L, Nista EC, Nucera E, Schiavino D, Patriarca G, Gasbarrini G, Pola P, Gasbarrini A. Idiopathic chronic urticaria and celiac disease. <i>Dig Dis Sci</i> 2005; <b>50</b>: 1702-1704</p>
</dt>
<dt>
<p>17. Hodgson HJ, Davies RJ, Gent AE, Hodson ME. Atopic disorders and adult coeliac disease presenting with symptoms of worsening astma. <i>Lancet</i> 1986; <b>2</b>: 1157-1158</p>
</dt>
<dt>
<p>18. Cooper BT, Holmes GK, Cooke WT. Coeliac disease and immunological disorders. <i>Br Med J</i> 1978; <b>1</b>: 537-539</p>
</dt>
<dt>
<p>19. Scala E, Giani M, Pirrotta L, Guerra EC, De Pita O, Puddu P. Urticaria and adult celiac disease. <i>Allergy</i> 1999; <b>54</b>: 1008-1009</p>
</dt>
<dt>
<p>20. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Pedrosa%20Delgado%20M%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Pedrosa Delgado M</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Mart%C3%ADn%20Mu%C3%B1oz%20F%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Martín Muñoz F</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Polanco%20Allu%C3%A9%20I%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Polanco Allué I</b></a>, <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&amp;Cmd=Search&amp;Term=%22Mart%C3%ADn%20Esteban%20M%22%5BAuthor%5D&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_RVAbstractPlus"><b>Martín Esteban M</b></a>. Cold urticaria and celiac disease. <a href="http://www.ncbi.nlm.nih.gov/">J Investig Allergol Clin Immunol.</a> 2008;18(2):123-5.</p>
</dt>
<dt>
<p>21. Wojnarowska F, Marsden RA, Bhogal B, Black MM. Chronic bullous disease of childhood, childhood cicatricial pemphigoid, and linear IgA disease of adults. A comparative study demonstrating clinical and immunopathologic overlap. <i>J Am Acad Dermatol</i> 1988; <b>19</b>: 792-805</p>
</dt>
<dt>
<p>22. Lawley TJ, Strober W, Yaoita H, Katz SI. Small intestinal biopsies and HLA types in dermatitis herpetiformis patients with granular and linear IgA skin deposits.<i> J Invest Dermatol</i> 1980; 74: 9-12</p>
</dt>
<dt>
<p>23. Chorzelski TP<strong>,</strong> Jablonska S. Diagnostic significance of the immunofluorescent pattern in dermatitis herpetiformis. <i>Int J Dermatol</i> 1975; 14: 429-436</p>
</dt>
<dt>
<p>24. Leonard JN, Griffiths CE, Powles AV, Haffenden GP, Fry L. Experience with a gluten free diet in the treatment of linear IgA disease. <i>Acta Derm Venereol</i> 1987; 67: 145-148</p>
</dt>
<dt>
<p>25. Egan CA, Smith EP, Taylor TB, Meyer LJ, Samowitz WS, Zone JJ. Linear IgA bullous dermatosis responsive to a gluten-free diet. <i>Am J Gastroenterol</i> 2001; 96: 1927-1929</p>
</dt>
<dt>
<p>26. Durand JM, Lefevre P, Weiller C. Erythema nodosum and coeliac disease. <i>Br J Dermatol</i> 1991; 125: 291-292</p>
</dt>
<dt>
<p>27. Bartyik K, Varkonyi A, Kirschner A, Endreffy E, Turi S, Karg E. Erythema nodosum in association with celiac disease. <i>Pediatr Dermatol</i> 2004; 21: 227-230</p>
</dt>
<dt>
<p>28. Douglas JG, Gillon J, Logan RF, Grant IW, Crompton GK. Sarcoidosis and coeliac disease: an association? <i>Lancet</i> 1984; 2: 13-15</p>
</dt>
<dt>
<p>29. Blackford S, Wright S, Roberts DL. Necrolytic migratory erythema without glucagonoma: the role of dietary essential fatty acids. <i>Br J Dermatol</i> 1991; 125: 460-462</p>
</dt>
<dt>
<p>30. Goodenberger DM, Lawley TJ, Strober W, Wyatt L, Sangree MH Jr, Sherwin R, Rosenbaum H, Braverman I, Katz SI. Necrolytic Migratory Erythema without glucagonoma: report of two cases. <i>Arch Dermatol</i> 1979; 115: 1429-1432</p>
</dt>
<dt>
<p>31. Kelly CP<strong>,</strong> Johnston CF, Nolan N, Keeling PW, Weir DG. Necrolytic migratory erythema with elevated plasma enteroglucagon in celiac disease. <i>Gastroenterology</i> 1989; 96: 1350-1353</p>
</dt>
<dt>
<p>32. Thorisdottir K, Camisa C, Tomecki KJ, Bergfeld WF. Necrolytic migratory erythema: a report of three cases. <i>J Am Acad Dermatol</i> 1994; 30: 324-329</p>
</dt>
<dt>
<p>33. Tasanen K<strong>,</strong> Raudasoja R, Kallioinen M, Ranki A. Erythema elevatum diutinum in association with coeliac disease. <i>Br J Dermatol</i> 1997; 136: 624-627</p>
</dt>
<dt>
<p>34.<strong>&#160;</strong>Collin P<strong>,</strong> Korpela M, Hallstrom O, Viander M, Keyrilainen O, Maki M. Rheumatic complaints as a presenting symptom in patients with coeliac disease. <i>Scand J Rheumatol</i> 1992; 21: 20-23</p>
</dt>
<dt>
<p>35. Rodriguez-Serna M, Fortea JM, Perez A, Febrer I, Ribes C, Aliaga A. Erythema elevatum diutinum associated with celiac disease: response to a gluten-free diet. <i>Pediatr Dermatol </i>1993; <b>10</b>: 125-128</p>
</dt>
<dt>
<p>36. Michaelsson G, Gerden B, Hagforsen E, Nilsson B, Pihl-Lundin I, Kraaz W, Hjelmquist G, Loof L. Psoriasis patients with antibodies to gliadin can be improved by a gluten-free diet. <i>Br J Dermatol</i> 2000; 142: 44-51</p>
</dt>
<dt>
<p>37. Cardinali C, Degl&#8217;innocenti D, Caproni M, Fabbri P. Is the search for serum antibodies to gliadin, endomysium and tissue transglutaminase meaningful in psoriatic patients? Relationship between the pathogenesis of psoriasis and coeliac disease. <i>Br J Dermatol</i> 2002; 147: 187-188</p>
</dt>
<dt>
<p>38. Woo WK, McMillan SA, Watson RG, McCluggage WG, Sloan JM, McMillan JC. Coeliac disease-associated antibodies correlate with psoriasis activity. <i>Br J Dermatol</i> 2004; 151: 891-894</p>
</dt>
<dt>
<p>39. Michaelsson G, Gerden B, Ottosson M, Parra A, Sjoberg O, Hjelmquist G, Loof L. Patients with psoriasis often have increased serum levels of IgA antibodies to gliadin. <i>Br J Dermatol</i> 1993; 129: 667-673</p>
</dt>
<dt>
<p>40.<strong>&#160;</strong>Addolorato G<strong>,</strong> Parente A, de Lorenzi G, D&#8217;angelo Di Paola ME, Abenavoli L, Leggio L, Capristo E, De Simone C, Rotoli M, Rapaccini GL, Gasbarrini G. Rapid regression of psoriasis in a coeliac patient after gluten-free diet. A case report and review of the literature. <i>Digestion</i> 2003; 68: 9-12</p>
</dt>
<dt>
<p>41. Abenavoli L, Leggio L, Ferrulli A, Vonghia L, Gasbarrini G, Addolorato G. Association between psoriasis and coeliac disease. <i>Br J Dermatol</i> 2005; 152: 1393-1394</p>
</dt>
<dt>
<p>42. Ojetti V, Aguilar Sanchez J, Guerriero C, Fossati B, Capizzi R, De Simone C, Migneco A, Amerio P, Gasbarrini G, Gasbarrini A. High prevalence of celiac disease in psoriasis. <i>Am J Gastroenterol</i> 2003; 98: 2574-2575</p>
</dt>
<dt>
<p>43. Damasiewicz-Bodzek A, Wielkoszynski T. Serologic Markers Of Celiac Disease In Psoriatic Patients. J Eur Acad Dermatol Venereol. 2008 Sep;22(9):1055-61.</p>
</dt>
<dt>
<p>44. Gorgos Diana. Patients With Psoriasis At Higher Risk For Celiac Disease. Dermatology Nursing June 1st, 2004.</p>
</dt>
<dt>
<p>45. Volta U, Bardazzi F, Zauli D, Defranceschi L, Tosti A, Molinaro N, Ghetti S, Tetta C, Grassi A, Bianchi FB. Serological Screening For Coeliac Disease In Vitiligo And Alopecia Areata. Br J Dermatol 1997 May;136(5):801-2.</p>
</dt>
<dt>
<p>46. Vitiligo: Autoimmune Silent and Non-Silent Celiac Sign. <cite>stanford.wellsphere.com/&#8230;/<b>vitiligo</b>-<b>autoimmune</b>-<b>silent-and-non</b>-<b>silent</b>&#8230;<b>sign</b>/736565 -</cite></p>
</dt>
<dt>
<p><cite></cite><cite>47. </cite>Collin P<strong>,</strong> Reunala T. Recognition and management of the cutaneous manifestations of celiac disease: a guide for dermatologist. <i>Am J Clin Dermatol</i> 2003; 4: 13-20</p>
</dt>
<dt>
<p>48. Reunala T, Collin P. Diseases associated with dermatitis herpetiformis. <i>Br J Dermatol</i> 1997; 136: 315-318</p>
</dt>
<dt>
<p>49. Triolo G, Triolo G, Accardo-Palumbo A, Carbone MC, Giardina E, La Rocca G. Behcet&#8217;s disease and coeliac disease. <i>Lancet </i>1995; 346: 1495</p>
</dt>
<dt>
<p>50. Buderus S, Wagner N, Lentze MJ. Concurrence of celiac disease and juvenile dermatomyositis: result of a specific immunogenetic susceptibility? <i>J Pediatr Gastroenterol Nutr</i> 1997; 25: 101-103</p>
</dt>
<dt>
<p>51. Falcini F<strong>,</strong> Porfirio B, Lionetti P. Juvenile dermatomyositis and celiac disease. <i>J Rheumatol</i> 1999; 26: 1419-1420</p>
</dt>
<dt>
<p>52. Marie I, Lecomte F, Hachulla E, Antonietti M, Francois A, Levesque H, Courtois H. An uncommon association: celiac disease and dermatomyositis in adults. <i>Clin Exp R</i><i>heumatol </i>2001; 19: 201-203</p>
</dt>
<dt>
<p>53. Iannone F<strong>,</strong> Lapadula G. Dermatomyositis and celiac disease association: a further case. <i>Clin Exp R</i><i>heumatol</i> 2001; 19: 757-758</p>
</dt>
<dt>
<p>54. Evron E, Abarbanel JM, Branski D, Sthoeger ZM. Polymyositis, arthritis, and proteinuria in a patient with adult celiac disease. <i>J Rheumatol</i> 1996; 23: 782-783</p>
</dt>
<dt>
<p>55. Mustajoki P, Vuoristo M, Reunala T. Celiac disease or dermatitis herpetiformis in three patients with porphyria. <i>Dig Dis Sci </i>1981; 26: 618-621</p>
</dt>
<dt>
<p>56. Twaddle S<strong>,</strong> Wassif WS, Deacon AC, Peters TJ. Celiac disease in patients with variegate porphyria. <i>Dig Dis Sci</i> 2001; 46: 1506-1508</p>
</dt>
<dt>
<p>57. Moore MR<strong>,</strong> Disler PB. Drug sensitive diseases-I-acute porphyrias. <i>Adverse Drug React Bull</i> 1988; 129: 484-487</p>
</dt>
<dt>
<p>58. Menni S<strong>,</strong> Boccardi D, Brusasco A. Ichthyosis revealing coeliac disease. <i>Eur J Dermatol</i> 2000; 10: 398-399</p>
</dt>
<dt>
<p>59. Schattner A<strong>.</strong> A 70-year-old man with isolated weight loss and a pellagra-like syndrome due to celiac disease. <i>Yale J Biol Med </i>1999; 72: 15-18</p>
</dt>
<dt>
<p>60. Lewis FM<strong>,</strong> Lewis-Jones S, Gipson M. Acquired cutis laxa with dermatitis herpetiformis and sarcoidosis. <i>J Am Acad Dermatol </i>1993; 29: 846-848</p>
</dt>
<dt>
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<p>62. Montalto M<strong>,</strong> Diociaiuti A, Alvaro G, Manna R, Amerio PL, Gasbarrini G. Atypical mole syndrome and congenital giant naevus in a patient with celiac disease. <i>Panminerva Med</i> 2003; 45: 219-221</p>
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<p>63. Wright DH. The major complications of coeliac disease. <i>Baillier</i><i>es Clin Gastroenterol</i> 1995; 9: 351-369</p>
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<p>64. Marghoob AA<strong>,</strong> Schoenbach SP, Kopf AW, Orlow SJ, Nossa R, Bart RS. Large congenital melanocytic nevi and the risk for the development of malignant melanoma. A prospective study. <i>Arch Dermatol</i> 1996; 132: 170-175</p>
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<p>66. Ackerman AB<strong>,</strong> Sood R, Koenig M. Primary acquired melanosis of the conjunctiva is melanoma in situ. <i>Mod Pathol</i> 1991; 4: 253-263</p>
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<p>67. Corazza GR<strong>,</strong> Masina M, Passarini B, Neri I, Varotti C. Ipetricosi lanuginosa acquisita associata a sindrome celiaca. <i>G Ital Dermatol Venereol</i> 1988; 123: 611-612</p>
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<p>68. Jones HJ<strong>,</strong> Mason DH. Oral manifestation of systemic disease. 2nd ed. London: Baillier Tindall, 1990.</p>
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<p>69. Ferguson R<strong>,</strong> Basu MK, Asquith P, Cooke WT. Jejunal mucosal abnormalities in patients with recurrent aphthous ulceration. <i>Br Med J</i> 1976; 1: 11-13</p>
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<p>70. Fortune F<strong>,</strong> Buchanan JA. Oral lichen planus and coeliac disease. <i>Lancet </i>1993; 341: 1154-1155</p>
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<p>72. Randle HW, Winkelmann RK. Pityriasis Rubra Pilaris And Celiac Sprue With Malabsorption. Cutis 1980 June;25(6):626-7</p>
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<p>74. Menni S, Boccardi D, Brusasco A. Ichthyosis Revealing Coeliac Disease. Eur J Dermatol 2000 Jul-Aug;10(5):398-9</p>
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<p>75. Green PH, Fleischauer AT, Bhagat G, Goyal R, Jabri B, Neugut AI. Risk Of Malignancy In Patients With Celiac Disease. Am J Med 2003 Aug 15;115(3):191-195</p>
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<p>77. Gislason SJ. Core Diet For Kids. Stephan J Gislason &amp; Environmed Research Inc. 1989.</p>
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<p>78. Feldman Mark, MD, Friedman Lawrence S, MD, Sleisenger, Marvin H, MD, Gastrointestinal and Liver Disease Pathophysiology/Diagnosis/Management 7th Edition, Volume11, 2002,Saunders</p>
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<p>79. Pruessner Harold T. Detecting Celiac Disease In Your Patients. American Family Physician. March 1st, 1998.</p>
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<p>80. <a title="http://sclero.org/medical/symptoms/associated/a-to-z.html" href="http://sclero.org/medical/symptoms/associated/a-to-z.html">http://sclero.org/medical/symptoms/associated/a-to-z.html</a> and <a title="http://sclero.org/medical/symptoms/associated/celiac-disease/a-to-z.html" href="http://sclero.org/medical/symptoms/associated/celiac-disease/a-to-z.html">http://sclero.org/medical/symptoms/associated/celiac-disease/a-to-z.html</a></p>
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<p>81. Gibney MJ, Marinos E, Olle L, Dowsett J. Clinical Nutrition. Blackwell Publishing 2005.</p>
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<p>82. Gibney MJ, Vorster HH, Kok FJ. Introduction to Human Nutrition. Blackwell Publishing 2002.</p>
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<p>83. Corazza GR, Andreani ML, Venturo N, Bernardi M, Tosti A, Gasbarrini G. Celiac disease And Alopecia Areata: Report Of A new Association. Gastroenterology 1995;109: 1333-1337.</p>
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<p>84. Naveh Y, Rosenthal E, Ben-Arieh Y, Etzioni A. Celiac Disease-Associated Alopecia In Childhood. J Pediatr 1999;134: 362-364.</p>
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<p>85. <a href="mailto:philippe.humbert@univ-fcomte.fr">Philippe Humbert</a><sup>1</sup>, Fabien Pelletier<sup>1</sup>, Brigitte Dreno<sup>2</sup>, Eve Puzenat<sup>1</sup>, François Aubin<sup>1</sup>.&#160; Gluten intolerance and skin diseases. European Journal Of Dermatology. Volume 16, Numéro 1, 4-11, January-February 2006.</p>
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<p>86. Balch Phyllis A. Prescription For Nutritional Healing. Penguin Group Inc., 2006.</p>
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<p>87. Fawcett Robert S, Linford Sean, Stulberg Daniel. Nail Abnormalities: Clues To Systemic Disease. March 15, 2004.</p>
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<p>88. Kagnoff MF. AGA Institute Medical Position Statement on the Diagnosis and Management of CD. Gastroenterology, Official Journal of the American Gastroenterological Association (AGA). December 2006.</p>
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<p>89. Alessio Fasano, M.D. Physiological, Pathological, and Therapeutic Implications of Zonulin-Mediated Intestinal Barrier Modulation. American Journal of Pathology, 2008;173:1243-1252.</p>
</p>
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		<title>Part 3 Of 12 Part Series: Sensory Symptoms (Vision, Hearing, Taste, Smell, and Touch) In Undiagnosed Celiac Disease.</title>
		<link>http://celiacnurse.com/sensory-symptoms-vision-hearing-taste-smell-and-touch-in-undiagnosed-celiac-disease/</link>
		<comments>http://celiacnurse.com/sensory-symptoms-vision-hearing-taste-smell-and-touch-in-undiagnosed-celiac-disease/#comments</comments>
		<pubDate>Fri, 11 Sep 2009 21:17:31 +0000</pubDate>
		<dc:creator>Shelly</dc:creator>
				<category><![CDATA[12 Part Series: CD Symptoms]]></category>

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		<description><![CDATA[This is the third in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, five sensory symptoms (vision, hearing, taste, smell, and touch) will be discussed. In many with undiagnosed CD, the intestinal villi, responsible for absorbing nutrients, becomes damaged, creating a flattened [...]]]></description>
			<content:encoded><![CDATA[<p>This is the third in a series of posts discussing the variety of symptoms that can be caused by undiagnosed Celiac Disease (CD). In this post, five sensory symptoms (vision, hearing, taste, smell, and touch) will be discussed. In many with undiagnosed CD, the intestinal villi, responsible for absorbing nutrients, becomes damaged, creating a flattened mucosal surface (villous flattening) that is less able to absorb nutrients. Autoimmune reactions to ingested gluten cross-react with intestinal villi and create this damage. Various nutrient deficiencies can occur and this, along with inflammation and other autoimmune factors, can lead to various sensory symptoms (8,71,72,74).&#160;<br />
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<h3><strong>Vision Symptoms</strong></h3>
<p>Functional vision is reliant on a healthy nervous system, vascular system, muscular system and structural eye integrity. Since these systems are dependent on nutrients, it is thought that vision loss may result from nutrient deficiencies that cause pathological changes in these systems. Multiple nutrient deficiencies can exist in CD and theoretically this along with autoimmune factors may cause a variety of symptoms. Vitamin A deficiency is well researched and can be common in CD. A deficiency is thought to be primarily responsible for many of the pathological changes that can occur to the conjunctiva, cornea, and retina. Some of the symptoms may only occur if the deficiency is chronic, this is probable in CD since misdiagnosis can occur for years (1,2,3,4,8,72,75).</p>
<p>Visual symptoms may include <strong>difficulty seeing in a dimly lit room, night blindness, conjunctival xerosis </strong>(dryness of the eye)<strong>, corneal xerosis</strong> (cornea rough, dry, and hazy)<strong>,</strong> <strong>keratoconjunctivitis sicca</strong> (dry cornea &amp; conjunctiva)<strong>, bitot’s spots </strong>(pearly foamy patch on conjunctiva and cornea)<strong>, keratomalacia </strong>(corneal necrosis, corneal ulceration)<strong>, corneal scar, formation of corneal opacity </strong>(cornea white or clouded over)<strong>, xerophthalmia </strong>(dry and inflamed eye)<strong>,</strong>&#160;<strong>xerophthalmic fundus</strong> (white or grey linear or oval opacities in the retina)<strong>, blindness, conjunctivitis with corneal vascularization and lens opacity, blepharitis</strong> (inflammation of the eyelids)<strong>,</strong> <strong>styes, and eye infections.</strong>&#160;<strong> </strong>As well,<strong> red (bloodshot) eyes</strong> or <strong>central retinal vein occlusion</strong> may occur if coagulation problems exist (1,3,4,76,78,87). </p>
<p><strong>Optic neuropathy</strong> is another complication that could arise from nutritional deficiencies. Symptoms usually present <strong>symmetrically and simultaneously, and are not painful</strong>. One eye may have visual symptoms prior to the other, but symptoms in the other should follow. <strong>Dyschromatopsia (defect in color vision)</strong> may be the first symptom. Colors (one or more) may not seem as bright and vivid as they were previously. <strong>Foggy, cloudy, or blurred vision</strong> may occur and may be more prevalent at the point of fixation. Vision may deteriorate rapidy. <strong>Centrocecal or central scrotomas (blind spots)</strong> may also occur (2). </p>
<p>Vision symptoms resulting from muscular problems could occur. <strong>Ocular myopathy</strong> in a 12 year old girl with CD has been documented. The ocular myopathy corrected itself with a gluten-free diet and vitamin supplementation (86). In theory, <strong>extraocular palsy and nystagmus</strong> could also occur due to a thiamine deficiency causing a central nervous system lesion (2). </p>
<p>There may also be a correlation between CD, <strong>macular degeneration and cataracts</strong> since these conditions tend to improve with supplementation of nutrients, such as vitamins A, C, E, zinc, lutein, zeaxanthin, and omega #3 (when they are given collectively) (6,77). Perhaps individuals who show improvement with supplementation suffer from malabsorption issues with CD. More research is needed. </p>
<p>Nutrient deficiencies contributing to the above symptoms can include vitamin <strong>A, B complex, C, E, K, zinc, copper, iron, taurine, and essential amino and fatty acids </strong>(1,2,3,4,5,7). More research is needed to specifically identify which nutrients are directly involved in each visual symptom and to investigate how common each symptom is in CD.</p>
<p><em>My visual symptoms included night blindness, blurred vision, bitot’s spots, flashes of light, occasional partial loss of vision (I was told this was likely due to ocular migraines), and periodically it appeared as if a cloud of fog was in the room. I also suffered occasionally from styes, and dry eyelids. I used prescription glasses in University to see the blackboard and to drive. I have perfect vision now and do not require glasses. My mother, also with CD, has some visual impairment and wears glasses. </em></p>
<h3><strong>Auditory (Hearing) Symptoms</strong></h3>
<p>Functional hearing is reliant on a healthy nervous system, vascular system, and skeletal system. Since these systems are dependent on nutrients, it is theorized that hearing loss may result from nutrient deficiencies that cause pathological changes in these systems (9-14). Multiple nutrient deficiencies can exist in CD and theoretically this may cause a variety of symptoms.</p>
<p>In humans and animals with nutritional deficiencies many types of auditory dysfunction has occurred (14,17). Auditory symptoms associated with possible malabsorption in CD could include <strong>tinnitis or ringing in the ears</strong> (14,15,23), <strong>auditory hallucinations </strong>(14,16), <strong>middle ear infections,</strong> <strong>loss of hearing,</strong> <strong>dizziness</strong>, <strong>and other hearing impairments</strong> (14). </p>
<p>In <strong>human studies,</strong> <strong>v</strong><strong>itamin A (3,4), B-12</strong> (14,18-21,60), <strong>folate</strong> (14,22-26,60), <strong>vitamin D</strong> (14,27-33), <strong>calcium</strong> (34,35), and <strong>iron</strong> (7,36,37) deficiency is associated with an alteration in hearing (14). In <strong>animal studies</strong> <strong>vitamin B-12</strong> (39), <strong>thiamine </strong>(40), <strong>riboflavin</strong> (40), <strong>vitamin B-6</strong> (40-44), <strong>vitamin A</strong> (40), <strong>vitamin C</strong> (40,45), <strong>vitamin D</strong> (40,46-48), <strong>vitamin E</strong> (40,49), <strong>copper</strong> (50), <strong>iron</strong> (38,51-54), <strong>magnesium</strong> (55-58), and <strong>zinc</strong> (59) deficiencies have had various effects on hearing (14).</p>
<p><em>I had intermittent tinnitis, and at times it felt like my hearing abilities would decline for a few minutes (sometimes up to a </em>half hour), then return. </p>
<h3><strong>Olfactory (Smell) And Gustatory (Taste) Symptoms</strong></h3>
<p>It is thought that nutrients are important for gustatory and olfactory function since the epithelial cells in these areas have high metabolic needs. More research is needed to identify specific nutrient requirements. <strong>Vitamin A</strong> (63,64,65), <strong>thiamine </strong>(3,4,14,62), <strong>riboflavin</strong> (63), <strong>pantothenic acid</strong> (63), <strong>pyridoxine</strong> (63), <strong>niacin </strong>(63), <strong>cobalamin </strong>(14,62), <strong>folic acid</strong> (63), <strong>vitamin</strong> E (63,79), <strong>copper</strong> (63,67,79) <strong>iodine</strong> (63,68),<strong> iron</strong> (63,78), <strong>zinc</strong> (63,66), and <strong>nickel</strong> (66) deficiencies have been identified as possible contributing factors to smell and taste impairments (63). Since all of these nutrients can be deficient in CD, taste and smell impairments may be possible. </p>
<p>Theoretically, CD olfactory (smell) symptoms could include <strong>anosmia (unable to smell), hyposmia (decreased detection of odours), dysosmia (incorrect identification of odours), parosmia (perception of smell is altered), phantosmia (false odour detected), agnosia (can smell, but difficulty in identifying odour)</strong>. Taste symptoms affecting the 5 tastes (salty, sweet, bitter, sour, and umami) could include <strong>ageusia (unable to taste), hypogeusia (decreased taste function), or dysgeusia (taste function is distorted/altered).</strong> If gustatory and olfactory senses are impaired, then <strong>appetite may be decreased</strong> leading to further malnutrition (66). Other symptoms may include <strong>lesions in the oral mucosa</strong> (esp. dorsal tongue), <strong>dry nose and mouth</strong>, <strong>papillary atrophy and degeneration</strong> <strong>of the tongue, atrophic glossitis, or pica cravings</strong> (63).&#160; </p>
<p><em>I found that I couldn’t smell as well as others. I often had a strange taste in my mouth (like metallic tin) and a bad breath taste that I couldn’t get rid of with mouthwash. Occasionally, I would experience phantosmia. Once eating gluten-free, these symptoms disappeared. </em></p>
<h3><strong>Touch Symptoms</strong></h3>
<p>Peripheral neuropathy can be the only symptom in CD and can occur without bowel symptoms or weight loss (70). Symptoms can include <strong>burning, tingling, numbness, or a loss of feeling in the hands and feet. These sensations can spread to the arms, legs, face, and body. Pain may also occur and may feel like an electric shock. Some feel an increased sensitivity to touch</strong> (70,80,81). As well, many other neurological symptoms can occur with CD. These additional symptoms will be discussed under the post about neurological symptoms.</p>
<p>Nutrient deficiencies contributing to peripheral neuropathy can include <strong>vitamins E, B complex, amino and fatty acids, calcium, magnesium, phosphorus, copper, electrolytes, and inositrol</strong>. Malabsorption of these nutrients in CD can lead to these symptoms (3,4,79,81,82). </p>
<p><em>I had intermittent tingling, numbness, vibrations, cold and burning feelings, and pain in my head, face, arms, and legs. I also had carpal tunnel for awhile and had to wear a brace. My daughter had tingling and numbness in her feet. These symptoms have disappeared now.</em></p>
<h3><strong>Other Influencing Factors</strong></h3>
<p>Other factors that may contribute to sensory symptoms are diabetes (diabetic retinopathy and neuropathy), certain medications, occupational exposures, smoking, diet, past eye surgery, age, low or high blood pressure, increased homocysteine levels, upper respiratory infections, trauma, infections, alcoholism, certain medications, candiasis, gingivitis, genetic differences, and brain surgery. The presence of other&#160; autoimmune diseases or conditions, such as scleroderma, downs syndrome, alzheimer&#8217;s disease, huntington&#8217;s disease, multiple sclerosis, parkinson&#8217;s dementias, idiopathic parkinson&#8217;s disease, complex of guam, epilepsy, age, muti-infarct dementia, schizophrenia, tumors, lupus, crohn’s disease, kidney disease, liver disease, or hypothyroidism can add to the symptoms (1,2,8,10,14,61,62,63,80,81). </p>
<h3><strong>Do You Have Any Of The Above Symptoms?</strong></h3>
<p><strong>Many individuals with undiagnosed CD will have no bowel symptoms </strong>(3,4). <strong>Weight loss may or may not occur, and is dependent on the amount of the intestine that is damaged </strong>(72,75,83). Therefore, the symptoms in this post could occur in the absence of weight loss or bowel symptoms. </p>
<p>The presence of sensory symptoms as discussed in this post, indicates that you should <strong>talk to your MD about</strong> <strong>tests for CD and tests to rule out other possible causes of your symptoms.</strong> Testing for CD is important because undiagnosed CD increases the risk of developing other autoimmune diseases, lymphomas (skin, brain, lymph nodes, intestine), cancers (thyroid, esophageal, mouth, tongue, pharynx, tonsil, and small intestine), allergies, complications from malabsorption issues, possible decreased immune response to other illnesses (8,72,75,84,85), and many other health complications that will be discussed in the posts about CD symptoms. It is my hope that if you have sensory symptoms, you can print out this post complete with medical references to take with you to the MD when you request a CD test. Highlight or underline the sections that apply to your symptoms. I’ll be posting a simplified summary and checklist in the 12th post. </p>
<p><strong>I recommend waiting until CD testing is complete before initiating a gluten-free diet because it may create a false negative. Discuss this with your MD or specialist. <strong>USE CAUTION WITH SUPPLEMENTS. </strong>Toxicities can occur with over supplementation and this can lead to permanent damage. Consult your MD, Registered Dietitian, or other medical specialists involved in your care to determine which nutrients should be supplemented and to identify appropriate dosages for you.</strong> <strong>Review your symptoms and everything in this post with a Medical Doctor</strong> <strong>and your specialists before you make any changes</strong>. <strong>Your MD knows your medical history and the treatments that are appropriate for you. </strong></p>
<h3><strong>References</strong></h3>
<p>1. Semba Richard D. Handbook Of Nutrition And Ophthalmology. Humana Press, 2007.</p>
<p>2. Miller Neil R., Walsh Frank Burton, Biousse Valérie, Hoyt William Fletcher. Walsh And Hoyt’s Clinical Neuro-Ophthalmology. Lippincott Williams And Wilkins, 2004.</p>
<p>3. Gibney MJ, Vorster HH, Kok FJ. Introduction to Human Nutrition. Blackwell Publishing 2002.</p>
<p><cite>4. Gibney MJ, Marinos E, Olle L, Dowsett J. Clinical Nutrition. Blackwell Publishing 2005.</cite></p>
<p><cite></cite><cite>5. <a title="http://www.webmd.com/eye-health/night-vision-problems-halos-blurred-vision-night-blindness" href="http://www.webmd.com/eye-health/night-vision-problems-halos-blurred-vision-night-blindness">http://www.webmd.com/eye-health/night-vision-problems-halos-blurred-vision-night-blindness</a> </cite></p>
<p><cite></cite><cite>6. Antinoro Linda. Sharpen All Five Of Your Senses By Eating Better, Smarter. Environmental Nutrition. May 1st, 2003.</cite></p>
<p><cite></cite><cite>7. Iron deficiency could Affect Hearing And Vision. Decision News Media SAS, May 7th, 2001.</cite></p>
<p><cite></cite><cite>8. <strong>Excellent Book:</strong> Green PHR, Jones, R. Celiac Disease A Hidden Epidemic. Collins, Harper Collins Publishers, 2006</cite></p>
<p><cite></cite><cite>9. Clark K, Sowers MR, Wallace RB, Jannausch ML, Lemke J, Anderson CV. Age-Related Hearing Loss And Bone Mass In A Population Of Rural Woman aged 60-85 yrs. Ann Epidemiol 1995;5:8-14.</cite></p>
<p><cite></cite><cite>10. Gates G., Cobb J., D’Agostino R., Wolf P. The Relation Of Hearing In The Elderly To The Presence Of Cardiovascular Disease And Cardiovascular Risk Factors. Arch Otolaryngol Head Neck Surg.1993;119:156-161.</cite></p>
<p><cite></cite><cite>11. Makishima K. Anterior Sclerosis As A Cause Of Presbycusis. Otolaryngology, 1978;86:322-326.</cite></p>
<p><cite></cite><cite>12. Seidman MD, Khan MJ, Dolan DF, Quirk WS. Age-Related Differences In Cochlear Microcirculation And Auditory Brain Stem Response. Arch Otolaryngol Head Neck Surg 1996;122:1221-1226.</cite></p>
<p><cite></cite><cite>13. Willot JF. Aging And The Inner Ear Of Animals. In: Aging And The Auditory System. Singular Publishing Group, Inc., San Diago, CA 1991:18-55.</cite></p>
<p><cite></cite><cite>14. Bales Connie W., Ritchie Christine S. Handbook Of Clinical Nutrition And Aging. Humana Press, 2003.</cite></p>
<p><cite></cite><cite>15. Nexo E, Hansen M, Rasmussen K, Lindgren A, Gräsbeck R. How To Diagnose Cobalamin Deficiency. Scand J Clin Lab Invest 1994;54:61-76.</cite></p>
<p><cite></cite><cite>16. Hector M, Burton JR. What Are The Psychiatric Manifestations Of B-12 Deficiency? J Am Geriatr Soc 1988;36:1105-1112. </cite></p>
<p><cite></cite><cite>17. Porter KH. Age-Related Hearing Loss And Nutrition In Older Women. Dissertation. University of Georgia, 1999.</cite></p>
<p><cite></cite><cite>18. Healton EB, Savage MD, Brust JCM, Garrett TJ, Lindenbaum MD. Neurologic Aspects Of Cobalamin Deficiency. Medicine 1991;70:229-245.</cite></p>
<p><cite></cite><cite>19. Krumholz A, Weiss HD, Goldstein PJ, Harris KC. Evoked Responses In Vitamin B-12 Deficiency. Ann Neurol 1981;9:407-409.</cite></p>
<p><cite></cite><cite>20. Fine EJ, Hallett M. Neurophysiological Study Of Subacute Combined Degeneration.&#160; J Neurol Sci 1980;45:331-336.</cite></p>
<p><cite></cite><cite>21. Fine EJ, Soria E, Paroski MW, Petryk D, Thomasula L. The Neurophysiological Profile Of Vitamin B-12 Deficiency. Muscle Nerve 1990;13:158-164.</cite></p>
<p><cite></cite><cite>22. Houston DK, Johnson MA, Nozza RJ, Gunter EW, Shea KJ, Cutler GM, Edmonds TJ. Age-Related Hearing Loss, Vitamins B-12 And Folate In Elderly Women. Am J Clin Nutr 1999;69:564-571.</cite></p>
<p><cite></cite><cite>23. Shemesh Z, Attias J, Ornan M, Shapira N, Shahar A. Vitamin B-12 Deficiency In Patient’s With Chronic Tinnitis And Noise Induced Hearing Loss. AM J Otolaryngol 1993;2:94-99.</cite></p>
<p><cite></cite>24. Berner B, Odem L, Parving A. Age-Related Hearing Impairment And B Vitamin Status. Acta Otolaryngol 2000;120:633-637.</p>
<p>25. Roman GC, An Epidemic In Cuba Of Optic Neuropathy, Sensorineural Deafness, Peripheral sensory neuropathy And Dorsallateral Myeloneuropathy. J Neurol Sci 1994;127:11-28.</p>
<p>26. DeNoon Daniel J. Folic Acid may Slow Hearing loss. 2007 WebMD. <a href="http://www.webmd.com">www.webmd.com</a></p>
<p>27. Horner K. Review: Morphological Changes Associated With Endolymphatic Hydrops. Scanning Microsc 1993;7:223-238.</p>
<p>28. Sewell WF. Neurotransmitters And Synaptic Transmission. In: The Cochlea. Dallos P, Popper AN, Fay RR (eds). Springer-verlag, New York, 1996 pp501-533.</p>
<p>29. <em>Sørensen</em>, MS. Temporal Bone Dynamics, The Hard Way. Acta Otolaryngol 1994;512:6-22.</p>
<p>30. <em>Sørensen</em> MS, Bretlau P, Jorgensen B. Quantum Type Bone Remodelling In The Human Otic Capsule. Acta Otolaryngol 1992A;496:4-10.</p>
<p>31. <em>Sørensen</em> MS, Bretlau P, Jorgensen B. Bone Remodelling In The Human Otic Capsule. Acta Otolaryngol 1992B;496:11-19.</p>
<p>32. <em>Sørensen</em> MS, Bretlau P, Jorgensen B. Fatigue Microdamage In Perilabyrinthine Bone. Acta Otolaryngol 1992C;496:20-27.</p>
<p>33. Wangemann P, Schacht J. Homeostatic Mechanisms In: The Cochlea. Dallos P, Popper AN, Fay RR (eds). Springer-verlag, New York, 1996, 130-185.</p>
<p>34. Women With Hearing Loss May Benefit By Boning Up On Calcium. Environmental Nutr. Oct. 1998. P,8.</p>
<p>35. Hearing Loss And Nutrition. Timely Topics From The Department Of Human Nutrition. <a href="http://www.oznet.ksu.edu/dp_fnut/_timely/hearingloss.htm">Http://www.oznet.ksu.edu/dp_fnut/_timely/hearingloss.htm</a></p>
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