Familial Mediterranean Fever Mimicking Wilson's Disease: A Case Report

Basit Öğe Kaydı
dc.contributor.authorTuran, Caner
dc.contributor.authorKarakoyun, Miray
dc.contributor.authorEcevit, Cigdem Omur
dc.contributor.authorYilmaz, Funda
dc.contributor.authorAydogdu, Sema
dc.date.accessioned2019-10-27T10:03:09Z
dc.date.available2019-10-27T10:03:09Z
dc.date.issued2018
dc.departmentEge Üniversitesien_US
dc.description.abstractWilson's disease (hepatolenticular degeneration) is an autosomal recessive defect in cellular copper transport. Impaired biliary copper excretion leads to an accumulation of copper mostly in the liver, brain and cornea. Familial Mediterranean Fever (FMF) is an autosomal recessive autoimmune disease as a result of a mutation in the MEFV gene encoding pyrin protein characterized by recurring fever and polyserositis attacks. In this report, we describe a Turkish female child with cholestatic hepatitis of unknown etiology who was later diagnosed with typical FMF.en_US
dc.identifier.doi10.4274/jpr.63308
dc.identifier.endpage155en_US
dc.identifier.issn2147-9445
dc.identifier.issn2147-9445en_US
dc.identifier.issue3en_US
dc.identifier.startpage153en_US
dc.identifier.urihttps://doi.org/10.4274/jpr.63308
dc.identifier.urihttps://hdl.handle.net/11454/30077
dc.identifier.volume5en_US
dc.identifier.wosWOS:000443041100010en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherGalenos Yayinciliken_US
dc.relation.ispartofJournal of Pediatric Researchen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectFamilial Mediterranean Feveren_US
dc.subjectWilson's diseaseen_US
dc.subjectliveren_US
dc.subjectcryptogenic cirrhosisen_US
dc.subjectcholestasisen_US
dc.titleFamilial Mediterranean Fever Mimicking Wilson's Disease: A Case Reporten_US
dc.typeArticleen_US

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