A Case of Henoch-Schönlein Purpura with P369S Mutation in MEFV Gene

BACKGROUND: Henoch-Schönlein purpura (HSP) is the most common vasculitis of childhood. HSP can affect multiple organs presenting with a characteristic rash in most of the patients. Familial Mediterranean Fever (FMF) is an inherited inflammatory disease common in mediterranean populations. HSP is the...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Ertan, Pelin, Tekin, Gökhan, Şahin, Gülseren Evirgen, Kasırga, Erhun, Taneli, Fatma, Kandioğlu, Ali Riza, Sözeri, Betül
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Tehran University of Medical Sciences 2011
Gaiak:
Case Report
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3446153/
https://ncbi.nlm.nih.gov/pubmed/23056796
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