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...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i:BMC Neurol
Main Authors: Zhang, Ya-Ni, Gao, Yuan-Yuan, Yang, Si-Da, Cao, Bin-Bin, Zheng, Ke-Lu, Wei, Ping, Chen, Lian-Feng, Chen, Wen-Xiong
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2019
Fag:
Case Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6907138/
https://ncbi.nlm.nih.gov/pubmed/31830942
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-019-1536-7
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker