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

• Main Authors: Nahid Aslani (Author), Kosar Asnaashari (Author), Nima Parvaneh (Author), Mohammad Shahrooei (Author), Maryam Sotoudeh-Anvari (Author), Farhad Shahram (Author), Vahid Ziaee (Author)
• Format: Book
• Published: BMC, 2022-09-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background 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, genital, and/or gastrointestinal (GI) ulcers, episodic fever, musculoske...