A Novel BTK Gene Mutation in a Child With Atypical X-Linked Agammaglobulinemia and Recurrent Hemophagocytosis: A Case Report

X-linked agammaglobulinemia (XLA), caused by a mutation in the Bruton's tyrosine kinase (BTK) gene, is rarely reported in patients with recurrent hemophagocytic lymphohistiocytosis (HLH). This mutation leads to significantly reduced numbers of circulatory B cells and serum immunoglobulins in pa...

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Detalles Bibliográficos
Autores principales: Han, Shu-Ping, Lin, Yung-Feng, Weng, Hui-Ying, Tsai, Shih-Feng, Fu, Lin-Shien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6711359/
https://www.ncbi.nlm.nih.gov/pubmed/31481959
http://dx.doi.org/10.3389/fimmu.2019.01953

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6711359/
https://www.ncbi.nlm.nih.gov/pubmed/31481959
http://dx.doi.org/10.3389/fimmu.2019.01953

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