X-Linked Agammaglobulinemia Leading to Chronic Obstructive Lung Disease

X-linked agammaglobulinemia (XLA) is a rare primary immunodeficiency disorder. It occurs in around one in 200,000 live births and is caused by mutations in the Bruton Tyrosine Kinase (BTK) gene leading to B lymphocyte deficiency and increased susceptibility to infection. Infection is the most common...

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Detalles Bibliográficos
Autores principales: Bean, Paris, Jani, Pushan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Infectious Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835111/
https://www.ncbi.nlm.nih.gov/pubmed/36644069
http://dx.doi.org/10.7759/cureus.32470

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835111/
https://www.ncbi.nlm.nih.gov/pubmed/36644069
http://dx.doi.org/10.7759/cureus.32470

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