Wiskott-Aldrich Syndrome

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.

Also Known As:

Eczema-Thrombocytopenia-Immunodeficiency Syndrome; Imd2; Immunodeficiency 2; Wiskott Syndrome; Eczema Thrombocytopenia Immunodeficiency Syndrome; Eczema-Thrombocytopenia-Immunodeficiency Syndromes; Immunodeficiency 2s; Wiskott Aldrich Syndrome; Wiskott Syndromes; Aldrich Syndrome

Hemic and Lymphatic Diseases: 7
- Hematologic Diseases: 3445
  - Cytopenia: 2659
    - Leukopenia: 5923
      - Lymphopenia: 4830
        Wiskott-Aldrich Syndrome: 714
  - Hemorrhagic Disorders: 706
    - Wiskott-Aldrich Syndrome: 714
  - Blood Coagulation Disorders: 168
    - Inherited Blood Coagulation Disorders: 76
      - Wiskott-Aldrich Syndrome: 714
  - Leukocyte Disorders: 8
    - Leukopenia: 5923
      - Lymphopenia: 4830
        Wiskott-Aldrich Syndrome: 714
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Primary Immunodeficiency Diseases: 1211
    - Wiskott-Aldrich Syndrome: 714
  - Inherited Blood Coagulation Disorders: 76
    - Wiskott-Aldrich Syndrome: 714
  - X-Linked Genetic Diseases: 42
    - Wiskott-Aldrich Syndrome: 714
Immune System Diseases: 4430
- Immunologic Deficiency Syndromes: 91
  - Lymphopenia: 4830
    - Wiskott-Aldrich Syndrome: 714
  - Primary Immunodeficiency Diseases: 1211
    - Wiskott-Aldrich Syndrome: 714

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