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Article

Clinical, laboratory and molecular characteristics of children with Familial Mediterranean Fever-associated vasculitis.

Acta paediatrica (Oslo, Norway : 1992) - 1 Feb 2000

Tekin M, Yalçinkaya F, Tümer N, Akar N, Misirlioğlu M, Cakar N

Abstract excerpt

Familial Mediterranean Fever (FMF) is an autosomal recessive disease characterized by recurrent self-limited attacks of fever accompanied by peritonitis, pleuritis and arthritis. Approximately 5% of individuals with FMF have been reported to have Henoch-Schönlein purpura (HSP) and about 1% have polyarteritis nodosa (PAN). Protracted febrile myalgia is another vasculitis-associated clinical entity among patients...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 10709887
DOI: 10.1080/080352500750028799

Genes

MEFV

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Clinical, laboratory and molecular characteristics of children with Familial Mediterranean Fever-associated vasculitis.PMID 10709887Read ↗

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