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dc.contributor.authorSaruhan-Direskeneli, Güher
dc.contributor.authorEraksoy, Mefkure
dc.contributor.authorYazici, Hasan
dc.contributor.authorGurvit, Hakan
dc.contributor.authorOge, Ali Emre
dc.contributor.authorAkman-Demir, Gulsen
dc.contributor.authorGul, Ahmet
dc.contributor.authorGurol, Edip
dc.contributor.authorOzdogan, Huri
dc.contributor.authorBahar, Sara
dc.date.accessioned2021-03-05T08:48:27Z
dc.date.available2021-03-05T08:48:27Z
dc.date.issued2006
dc.identifier.citationAkman-Demir G., Gul A., Gurol E., Ozdogan H., Bahar S., Oge A. E. , Gurvit H., Saruhan-Direskeneli G., Yazici H., Eraksoy M., "Inflammatory/demyelinating central nervous system involvement in familial Mediterranean fever (FMF): Coincidence or association?", Journal of Neurology, cilt.253, ss.928-934, 2006
dc.identifier.issn0340-5354
dc.identifier.othervv_1032021
dc.identifier.otherav_9acd8508-9cbd-42f9-ba85-94ee6c569806
dc.identifier.urihttp://hdl.handle.net/20.500.12627/104048
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33746257521&origin=inward
dc.identifier.urihttps://doi.org/10.1007/s00415-006-0137-8
dc.description.abstractFamilial Mediterranean fever (FMF) is an inherited inflammatory disease characterized by recurrent febrile polyserositis. Central nervous system (CNS) involvement in FMF is uncommon, but recently cases with multiple sclerosis (MS) and FMF have been reported. Here we assess patients with both FMF and MS, in order to clarify any relationship between FMF and MS, and to evaluate disease characteristics. Our MS database between 1986-2005 was screened retrospectively, and patients with both FMF and inflammatory/demyelinating CNS disease were evaluated among a total of 2800 patients including definite MS (n = 2268) and other demyelinating disorders. There were 12 patients with FMF, who developed a CNS disorder with multifocal white matter lesions. Median age at onset of FMF was 7 years, and median age at neurological onset was 26.8 years. Nine patients (including two siblings) had definite MS according to clinical and MRI findings, whereas 3 patients had atypical features suggesting other demyelinating disorders. Disease severity varied among the patients between very mild to a fatal course. All 8 patients evaluated for oligoclonal IgG bands in CSF were positive. The rate of FMF among our patients with definite MS is almost 4 times the expected prevalence in Turkey. Our series including a sibling pair concordant for FMF and MS may suggest that similar genetic susceptibility and environmental factors might be responsible, although coincidence still remains a possibility. A prospective study on a larger sample seems to be justified.
dc.language.isoeng
dc.subjectKlinik Tıp
dc.subjectNöroloji
dc.subjectDahili Tıp Bilimleri
dc.subjectKLİNİK NEUROLOJİ
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.titleInflammatory/demyelinating central nervous system involvement in familial Mediterranean fever (FMF): Coincidence or association?
dc.typeMakale
dc.relation.journalJournal of Neurology
dc.contributor.department, ,
dc.identifier.volume253
dc.identifier.issue7
dc.identifier.startpage928
dc.identifier.endpage934
dc.contributor.firstauthorID179081


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