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Syndrome

Wiskott-Aldrich Syndrome

AMW:DIS:150061

A rare, X-linked immunodeficiency syndrome characterized by ECZEMA; LYMPHOPENIA; and, recurrent pyogenic infection. It is seen exclusively in young boys. Typically, IMMUNOGLOBULIN M levels are low and IMMUNOGLOBULIN A and IMMUNOGLOBULIN E levels are elevated. Lymphoreticular malignancies are common.

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Wiskott-Aldrich Syndrome has parent Blood Coagulation Disorders, Inherited
Wiskott-Aldrich Syndrome has parent Genetic Diseases, X-Linked
Wiskott-Aldrich Syndrome has parent Hemorrhagic Disorders
Wiskott-Aldrich Syndrome has parent Lymphopenia
Wiskott-Aldrich Syndrome has parent Primary Immunodeficiency Diseases

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