Egyszerű nézet

dc.contributor.author Soos Z
dc.contributor.author Salamon M
dc.contributor.author Erdei K
dc.contributor.author Kaszas N
dc.contributor.author Folyovich, András
dc.contributor.author Szűcs, Anna
dc.contributor.author Arányi, Zsuzsanna
dc.contributor.author Winkler, Gábor
dc.date.accessioned 2015-02-21T20:05:29Z
dc.date.available 2015-02-21T20:05:29Z
dc.date.issued 2014
dc.identifier 84903164961
dc.identifier.citation pagination=205-209; journalVolume=67; journalIssueNumber=5-6; journalTitle=IDEGGYÓGYÁSZATI SZEMLE / CLINICAL NEUROSCIENCE;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/1273
dc.description.abstract Celiac disease--in its typical form--is a chronic immune-mediated enteropathy with typical clinical symptoms that develops against gliadin content of cereal grains, and is often associated with other autoimmune diseases. In cases of atypical manifestation classic symptoms may be absent or mild, and extra-intestinal symptoms or associated syndromes dominate clinical picture. The authors present a longitudinal follow-up of such a case. A 63-years old woman was diagnosed with epilepsy at the age of 19, and with progressive limb ataxia at the age of 36, which was initially thought to be caused by cerebellar atrophy, later probably by stiff person syndrome. At the age 59, her diabetes mellitus manifested with type 2 diabetic phenotype, but based on GAD positivity later was reclassified as type 1 diabetes. Only the last check-up discovered the celiac disease, retrospectively explaining the entire disease course and neurological symptoms. By presenting this case, the authors would like to draw attention to the fact that one should think of the possibility of celiac disease when cerebellar ataxia, progressive neurological symptoms and diabetes are present at the same time. An early diagnosis may help to delay the progression of disease and help better treatment.
dc.relation.ispartof urn:issn:0019-1442
dc.title LADA type diabetes, celiac diasease, cerebellar ataxia and stiff person syndrome. A rare association of autoimmune disorders.
dc.type Journal Article
dc.date.updated 2015-01-29T14:01:04Z
dc.language.rfc3066 en
dc.identifier.mtmt 2735531
dc.identifier.pubmed 25087381
dc.contributor.department SE/AOK/K/Neurológiai Klinika
dc.contributor.institution Semmelweis Egyetem


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Egyszerű nézet