Review paper

Autosomic dominant familial Behçet disease and haploinsufficiency A20: A review of the literature

Volume: 17, Issue: 8, Pages: 809 - 815
Published: Aug 1, 2018
Abstract
Behçet disease (BD) is a systemic vasculitis involving vessels from any size with various clinical features. Most BD cases are multifactorial and associated with the HLA B51 antigen. In rare and severe early onset cases, dominant Mendelian transmission has been linked to mutations in the TNFAIP3 gene encoding A20. Herein, we propose a systematic review of the literature about the haploinsufficiency A20 (HA20) published cases.Our review of the 45...
Paper Details
Title
Autosomic dominant familial Behçet disease and haploinsufficiency A20: A review of the literature
Published Date
Aug 1, 2018
Volume
17
Issue
8
Pages
809 - 815
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