Late diagnosis of agammaglobulinemia in an 8-year-old boy

Chromosome X-linked Bruton agammaglobulinemia is classified as a primary immunodeficiency disorder. It is a genetic condition associated with a mutation in the BTK gene encoding tyrosine kinase. It is characterised by the lack or only trace amounts of B cells and immunoglobulins, which results in...

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Bibliographic Details
Main Authors: Małgorzata Sopińska, Karolina Kapusta, Edyta Heropolitańska-Pliszka, Anna Jung, Bolesław Kalicki
Format: Article
Language:English
Published: Medical Communications Sp. z o.o. 2016-06-01
Series:Pediatria i Medycyna Rodzinna
Subjects:
Online Access:http://www.pimr.pl/index.php/issues/2016-vol-12-no-2/late-diagnosis-of-agammaglobulinemia-in-an-8-year-old-boy?aid=962

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