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A mutation in the promoter region of BTK causes atypical XLA

X-linked Agammaglobulinemia is a primary immunodeficiency caused by mutations in BTK, a tyrosine kinase essential for B lymphocytes differentiation. Patients usually have very low or absent B lymphocytes and are not able to develop humoral specific responses. Here we present a boy, diagnosed with XL...

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Detalles Bibliográficos
Autores principales: Bravo García-Morato, María, del Pino Molina, Lucía, Torres Canizales, Juan Manuel, del Rosal Rabes, Teresa, Méndez Echevarría, Ana, González Martínez, Berta, López-Granados, Eduardo, Rodríguez Pena, Rebeca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501425/
https://www.ncbi.nlm.nih.gov/pubmed/32995611
http://dx.doi.org/10.1016/j.heliyon.2020.e04914
Descripción
Sumario:X-linked Agammaglobulinemia is a primary immunodeficiency caused by mutations in BTK, a tyrosine kinase essential for B lymphocytes differentiation. Patients usually have very low or absent B lymphocytes and are not able to develop humoral specific responses. Here we present a boy, diagnosed with XLA due to a mutation on the promoter region of the gene, whose phenotype is characterised by low percentage of B cells, hypogammaglobulinemia, oscillating neutropenia, antibodies responses to some antigens after vaccination and IgE-mediated allergy. Additional technology as flow cytometry was needed to demonstrate the pathological status of the variant. We focus on the idea that XLA should be suspected in males with B lymphopenia and hypogammaglobulinemia, even if they make humoral specific responses. We also highlight the importance of sequencing BTK's promoter region, as mutations on it can be disease-causing.