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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...
Sparad:
| I publikationen: | BMC Neurol |
|---|---|
| Huvudupphovsmän: | , , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
BioMed Central
2019
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| Ämnen: | |
| 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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