Agammaglobulinemia, alymphocytotic type: A rare inherited immunodeficiency disorder involving a lack of T and B lymphocytes which makes the patient susceptible to bacterial and viral infections. More detailed information about the symptoms, causes, and treatments of Agammaglobulinemia, alymphocytotic type is available below.
Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Agammaglobulinemia, alymphocytotic type as a "rare disease".
Source - Orphanet
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