Familial Mediterranean fever and ankylosing spondylitis: A case report

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dc.contributor.authorGüliter S.
dc.contributor.authorÖzkurt Z.N.
dc.contributor.authorKeleş I.
dc.contributor.authorKeleş H.
dc.contributor.authorAydin G.
dc.date.accessioned2020-06-25T15:13:29Z
dc.date.available2020-06-25T15:13:29Z
dc.date.issued2005
dc.departmentKırıkkale Üniversitesi
dc.description.abstractFamilial Mediterranean fever (FMF) is an inherited disease characterized by recurrent attacks of fever and accompanying peritonitis, pleuritis, arthritis or erysipelas-like skin disease. The relationship between FMF and spondyloarthropathy (SpA) remains controversial. We described a particular case of 36-yr-old male patient with FMF and ankylosing spondylitis with negative HLA-B27. This case had late-onset FMF in spite of homozygote M694V mutation and his typical acute attacks of FMF began many years after the initiation of complaints related to sacroiliitis. There is no general consensus on whether the association of FMF and SpA is only an occasional coincidence or they are clinically and pathologically linked two conditions. Further studies with larger series are required to clarify the relationship between FMF and SpA.en_US
dc.identifier.endpage205en_US
dc.identifier.issn13000691
dc.identifier.issue3en_US
dc.identifier.scopus2-s2.0-33845977713
dc.identifier.scopusqualityN/A
dc.identifier.startpage200en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12587/1822
dc.identifier.volume16en_US
dc.indekslendigikaynakScopus
dc.language.isoen
dc.relation.ispartofJournal of Rheumatology and Medical Rehabilitation
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAnkylosing spondylitisen_US
dc.subjectFamilial Mediterranean feveren_US
dc.subjectM694V mutationen_US
dc.subjectSpondyloarthropathyen_US
dc.titleFamilial Mediterranean fever and ankylosing spondylitis: A case reporten_US
dc.typeArticle

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