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...

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Bibliografiska uppgifter
I publikationen:BMC Neurol
Huvudupphovsmän: Zhang, Ya-Ni, Gao, Yuan-Yuan, Yang, Si-Da, Cao, Bin-Bin, Zheng, Ke-Lu, Wei, Ping, Chen, Lian-Feng, Chen, Wen-Xiong
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2019
Ämnen:
Case Report
Länkar: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
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