RECURRENT HENOCH-SCHÖNLEIN PURPURA IN FAMILIAL MEDITERRANEAN FEVER
Familial Mediterranean fever (FMF) is a relatively rare disorder, characterized by recurrent self-limited attacks of fever and polyserositis. Diagnosis is made by clinical features, gene identification on chromosome 16 and clinical response to specific treatment. Different types of vasculitis have b...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
Tehran University of Medical Sciences
2008-08-01
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Series: | Acta Medica Iranica |
Online Access: | https://acta.tums.ac.ir/index.php/acta/article/view/3497 |