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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.

Year introduced: 1985

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Tree Number(s): C15.378.100.100.970, C15.378.463.960, C15.378.553.546.605.900, C16.320.099.970, C16.320.322.937, C20.673.627.900

MeSH Unique ID: D014923

Entry Terms:

  • Syndrome, Wiskott-Aldrich
  • Wiskott Aldrich Syndrome
  • Wiskott Syndrome
  • Imd2
  • Immunodeficiency 2
  • Aldrich Syndrome
  • Syndrome, Aldrich
  • Eczema-Thrombocytopenia-Immunodeficiency Syndrome
  • Eczema Thrombocytopenia Immunodeficiency Syndrome
  • Eczema-Thrombocytopenia-Immunodeficiency Syndromes
  • Syndrome, Eczema-Thrombocytopenia-Immunodeficiency
  • Syndromes, Eczema-Thrombocytopenia-Immunodeficiency

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