Concurrent demyelinizing central nervous system involvement in a case of Familial Mediterranean Fever with the M694V mutation

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dc.contributor.authorOzkan, Adile
dc.contributor.authorKosar, Sule
dc.contributor.authorUludağ, Ahmet
dc.contributor.authorHaznedaroglu, Mete
dc.contributor.authorKaraman, Handan Isın Ozısık
dc.date.accessioned2025-01-27T19:04:18Z
dc.date.available2025-01-27T19:04:18Z
dc.date.issued2014
dc.departmentÇanakkale Onsekiz Mart Üniversitesi
dc.description.abstractFamilial Mediterranean Fever (FMF) is a hereditary disease seen mainly around the Mediterranean. The most common mutations are M694V, M680I, V726A and E148. Neurological findings and magnetic resonance imaging (MRI) abnormalities resembling multiple sclerosis have been reported in a few cases. We present a case where an M694V mutation was found together with familial Mediterranean fever and multiple sclerosis-type demyelinizing disease as this combination is rarely seen. © 2014, Yuzuncu Yil Universitesi Tip Fakultesi. All rights reserved.
dc.identifier.endpage201
dc.identifier.issn1301-0883
dc.identifier.issue4
dc.identifier.scopus2-s2.0-85013092910
dc.identifier.scopusqualityQ4
dc.identifier.startpage198
dc.identifier.urihttps://hdl.handle.net/20.500.12428/13902
dc.identifier.volume19
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherYuzuncu Yil Universitesi Tip Fakultesi
dc.relation.ispartofEastern Journal of Medicine
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_Scopus_20250125
dc.subjectDemyelinizing disease; Familial Mediterranean Fever; M694V mutation
dc.titleConcurrent demyelinizing central nervous system involvement in a case of Familial Mediterranean Fever with the M694V mutation
dc.typeArticle

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