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Article

Prevalence of MEFV gene mutations and their clinical correlations in Turkish children with Henoch-Schönlein purpura.

Acta paediatrica (Oslo, Norway : 1992) - 1 May 2011

Bayram Cengiz, Demircin Gülay, Erdoğan Ozlem, Bülbül Mehmet, Caltik Aysun, Akyüz Sare G

Abstract excerpt

AIM: To investigate the frequency of MEFV mutations and their associations with the clinical and laboratory findings in children with Henoch-Schönlein purpura (HSP). METHODS: One hundred and seven children with HSP were investigated for 12 common MEFV mutations. RESULTS: Forty-seven patients (43.9%) were found to have one of the MEFV mutations. Eight patients (7.5%) were homozygous for one mutation, 33 (30.8%)...

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Source

Identifiers

PMID: 21231959
DOI: 10.1111/j.1651-2227.2011.02143.x

Genes

MEFV
CRP

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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