X linked agammaglobulinaemia with a 'leaky' phenotype.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 8758136.
- Also identified by PMC identifier 1511560.
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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.
Medical subject headings
- Agammaglobulinemia
- Genetic Linkage
- X Chromosome