Article
Clinical, Immunological, and Genetic Features in Patients with Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) and IPEX-like Syndrome.
The journal of allergy and clinical immunology. In practice - 1 Sept 2020
Jamee Mahnaz, Zaki-Dizaji Majid, Lo Bernice, Abolhassani Hassan, Aghamahdi Fatemeh, Mosavian Mehdi, Nademi Zohreh, Mohammadi Hamed, Jadidi-Niaragh Farhad, Rojas Manuel, Anaya Juan-Manuel, Azizi Gholamreza
Abstract excerpt
BACKGROUND: Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is a rare inborn error of immunity caused by mutations in the forkhead box P3 (FOXP3) gene. OBJECTIVE: In this study, we conducted a systematic review of patients with IPEX and IPEX-like syndrome to delineate differences in these 2 major groups. METHODS: The literature search was performed in PubMed, Web of Science, and...
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