Agammaglobulinemia

Agammaglobulinemia is rare disorder that only affects male as it is inherited as an X-linked recessive trait (like hemophilia).
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X-linked agammaglobulinemia, also called Bruton's agammaglobulinemia or congenital agammaglobulinemia, was the first immunodeficiency disease ever identified.
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Agammaglobulinemia (very rare)
Amyloidosis
Leukemia
Preeclampsia
Increased levels of IgM may indicate the following: ...
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AGAMMAGLOBULINEMIA: Absence or low levels of the gamma fraction of serum globulin. Commonly used to describe absence of immunoglobulins in general. See Antibodies.
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CVID Acronym for common variable immunodeficiency; a.k.a. hypogammaglobulinemia, adult-onset agammaglobulinemia, acquired agammaglobulinemia. See definition provided by Human Genome Sciences, Inc.
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those for the enzyme steroid sulfatase, episodic muscle weakness, ocular albinism, Charcot-Marie-Tooth disease (one kind of this neurologic disease), retinoschisis (retinal splitting due to degeneration), infantile spasm syndrome, agammaglobulinemia ...
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