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Bruton agammaglobulinemia tyrosine kinaseA genetic type of immunodeficiency characterized by failure to produce mature B lymphocytes and gamma globulin, due to mutation (change) in the agammaglobulinemia tyrosine kinase gene situated on the X chromosome (in the region Xq21.3-q22). The disorder is inherited as an X-linked recessive trait. Patients are males with absent or minimal lymphoid [..]
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