Delayed diagnosis of X-linked agammaglobulinaemia in a boy with recurrent meningitis

BACKGROUND: X-linked agammaglobulinaemia (XLA) is a rare inherited primary immunodeficiency disease characterized by the B cell developmental defect, caused by mutations in the gene coding for Bruton’s tyrosine kinase (BTK), which may cause serious recurrent infections. The diagnosis of XLA is somet...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Ya-Ni, Gao, Yuan-Yuan, Yang, Si-Da, Cao, Bin-Bin, Zheng, Ke-Lu, Wei, Ping, Chen, Lian-Feng, Chen, Wen-Xiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6907138/
https://www.ncbi.nlm.nih.gov/pubmed/31830942
http://dx.doi.org/10.1186/s12883-019-1536-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6907138/
https://www.ncbi.nlm.nih.gov/pubmed/31830942
http://dx.doi.org/10.1186/s12883-019-1536-7

Ejemplares similares