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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Cureus
2022
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| 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 |