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

• Prif Awduron: Nahid Aslani (Awdur), Kosar Asnaashari (Awdur), Nima Parvaneh (Awdur), Mohammad Shahrooei (Awdur), Maryam Sotoudeh-Anvari (Awdur), Farhad Shahram (Awdur), Vahid Ziaee (Awdur)
• Fformat: Llyfr
• Cyhoeddwyd: BMC, 2022-09-01T00:00:00Z.
• Pynciau: article
• Mynediad Ar-lein: 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...