X-linked agammaglobulinemia
X-linked agammaglobulinemia (also called X-linked hypogammaglobulinemia, XLA, Bruton type agammaglobulinemia, Bruton syndrome, or Sex-linked agammaglobulinemia) is a rare X-linked genetic disorder discovered in 1952 that affects the body's ability to fight infection.
X-linked agammaglobulinemiaBruton's tyrosine kinaseAntibodyX-linked recessive inheritanceBtk-type zinc fingerIntravenous immunoglobulinHNRPH2Ogden BrutonSerologyHypogammaglobulinemiaList of cutaneous conditionsPrimary immunodeficiencyBTKList of diseases (B)XLAList of OMIM disorder codesIGLL1Humoral immune deficiencyImmune disorderCommon variable immunodeficiency
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