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Article

MEFV gene mutations in Egyptian children with Henoch-Schonlein purpura.

Pediatric rheumatology online journal - 1 Jan 2014

Salah Samia, Rizk Samia, Lotfy Hala M, El Houchi Salma, Marzouk Huda, Farag Yomna

Abstract excerpt

BACKGROUND: Due to an increased frequency of vasculitis in FMF patients, many investigators have studied MEFV mutations in patients with HSP. The aim of the study is to investigate the frequency and clinical significance of MEFV mutations in Egyptian children with Henoch-Schonlein purpura (HSP). Investigating MEFV mutations in controls may help in estimating the prevalence of MEFV mutation carrier rate in...

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Identifiers

PMID: 25232290
DOI: 10.1186/1546-0096-12-41
PMCID: PMC4165914

Genes

MEFV

Variants

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