A Novel STAT3 Mutation in a Patient with Hyper-IgE Syndrome Diagnosed with a Severe Necrotizing Pulmonary Infection

PURPOSE: Autosomal dominant hyper-IgE syndrome (HIES) is a rare primary immune deficiency syndrome caused mainly by mutations in the signal transducer and activator of transcription 3 (STAT3) gene. More information on STAT3 mutations is still needed, and further investigation is warranted. A girl wi...

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Detalles Bibliográficos
Autores principales: Zhao, Ran, Wang, Chao, Sun, Chao, Jiang, Kun, Wu, Shengnan, Pan, Fen, Zeng, Zeyu, Hu, Yijing, Dong, Xiaoyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966388/
https://www.ncbi.nlm.nih.gov/pubmed/33737815
http://dx.doi.org/10.2147/JAA.S295516

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966388/
https://www.ncbi.nlm.nih.gov/pubmed/33737815
http://dx.doi.org/10.2147/JAA.S295516

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