TNFAIP3 mutation causing haploinsufficiency of A20 with a hemophagocytic lymphohistiocytosis phenotype: a report of two cases

A20 haploinsufficiency (HA20) is a newly introduced autosomal dominant autoinflammatory disorder, also known as Behcet ’s-like disease. Some of the most common symptoms of the disease are recurrent oral, genita...

Source: Pediatric Rheumatology - September 5, 2022 Category: Rheumatology Authors: Nahid Aslani, Kosar Asnaashari, Nima Parvaneh, Mohammad Shahrooei, Maryam Sotoudeh-Anvari, Farhad Shahram and Vahid Ziaee Tags: Case Report Source Type: research