X linked agammaglobulinaemia with a 'leaky' phenotype

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Abstract

Typical X linked agammaglobulinaemia (XLA) is characterised by absence of immunoglobulin production and lack of mature B cells. The gene responsible for XLA has recently been identified, and codes for a B cell tyrosine kinase, BTK. A family affected by a B cell immunodeficiency, which is less severe than classical XLA, is described but they had a pedigree suggestive of X linked inheritance. Demonstration of a mutation in the BTK gene confirms that this is a mild form of XLA.

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Jones, A., Bradley, L., Alterman, L., Tarlow, M., Thompson, R., Kinnon, C., & Morgan, G. (1996). X linked agammaglobulinaemia with a “leaky” phenotype. Archives of Disease in Childhood, 74(6), 548–549. https://doi.org/10.1136/adc.74.6.548

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