Clinical and immunological characteristics of five patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China–expanding the atypical phenotypes

BACKGROUND: Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is a rare disorder of the immune regulatory system caused by forkhead box P3 (FOXP3) mutations. Abnormal numbers or functions of regulatory T (Treg) cells account for the various autoimmune symptoms. We aimed...

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Detalles Bibliográficos
Autores principales: Huang, Yu, Fang, Shuyu, Zeng, Ting, Chen, Junjie, Yang, Lu, Sun, Gan, Dai, Rongxin, An, Yunfei, Tang, Xuemei, Dou, Ying, Zhao, Xiaodong, Zhou, Lina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9448973/
https://www.ncbi.nlm.nih.gov/pubmed/36091011
http://dx.doi.org/10.3389/fimmu.2022.972746

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9448973/
https://www.ncbi.nlm.nih.gov/pubmed/36091011
http://dx.doi.org/10.3389/fimmu.2022.972746

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