Bruton-type agammaglobulinemia

X-linked agammaglobulinemia (XLA) is a clinically variable form of isolated agammaglobulinemia, an inherited immunodeficiency disorder, and is characterized in affected males by recurrent bacterial infections during infancy.

Also known as: BTK-deficiency, Bruton type agammaglobulinemia, Bruton's Sex-linked agammaglobulinemia, Bruton's X-linked agammaglobulinemia, Bruton-type agammaglobulinemia, X-linked agammaglobulinemia, agammaglobulinemia, X-linked 1, X-linked recessive, Bruton's agammaglobulinemia

91 clinical trials for this condition and its sub-types.