Primary agammaglobulinemia: A genetic disorder characterized by a deficiency of antibodies due to abnormal development of B lymphocytes. More detailed information about the symptoms, causes, and treatments of Primary agammaglobulinemia is available below.
See full list of 14 symptoms of Primary agammaglobulinemia
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Primary agammaglobulinemia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Primary agammaglobulinemia, or a subtype of Primary agammaglobulinemia,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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