Hyperimmunoglobulin D Syndrome: Case Report

dc.contributor.authorŞen, Hacer
dc.contributor.authorSılan, Fatma
dc.contributor.authorBinnetoğlu, Emine
dc.contributor.authorGüneş, Fahri
dc.contributor.authorAkurut, Çisem
dc.contributor.authorUludağ, Ahmet
dc.contributor.authorÖzdemir, Öztürk
dc.date.accessioned2025-01-27T19:48:47Z
dc.date.available2025-01-27T19:48:47Z
dc.date.issued2015
dc.departmentÇanakkale Onsekiz Mart Üniversitesi
dc.description.abstractHyperimmunoglobulin D syndrome is a rare autosomal recessive inherited disease characterized by fever attacks, which may be accompanied by chills, headache, abdominal pain, and cervical lymphadenopathy. Typical hyperimmunoglobulin D syndrome patients start to show symptoms in the first years of life. Diagnosis is based on the presence of symptoms with reduction in the enzyme activity of mevalonate kinase or by detecting the mutation in the mevalonate kinase gene that causes the disease. In this article, we present a 21-year-old female patient who started having fever attacks in early childhood and was diagnosed with familial Mediterranean fever; however, in spite of treatment, whose complaints did not resolve. The genetic analysis, which detected homozygote mevalonate kinase gene mutation and resulted in the hyperimmunoglobulin D syndrome diagnosis, is presented with an accompanying discussion of the literature.
dc.identifier.endpage246
dc.identifier.issn2148-5046
dc.identifier.issn2618-6500
dc.identifier.issue3
dc.identifier.startpage244
dc.identifier.trdizinid177804
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/177804
dc.identifier.urihttps://hdl.handle.net/20.500.12428/18866
dc.identifier.volume30
dc.indekslendigikaynakTR-Dizin
dc.language.isoen
dc.relation.ispartofArchives of Rheumatology
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_TRD_20250125
dc.subjectGenel ve Dahili Tıp
dc.subjectRomatoloji
dc.titleHyperimmunoglobulin D Syndrome: Case Report
dc.typeArticle

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