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MeSH 搜索器

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.
推出的年份: 1985
副标题
树号: C15.378.100.100.970, C15.378.463.960, C15.378.553.546.605.900, C16.320.099.970, C16.320.322.937, C16.320.798.875, C20.673.627.900, C20.673.795.875
MeSH 单一 ID: D014923
进入的组:
  • Wiskott Aldrich Syndrome
  • Wiskott Syndrome
  • Wiskott Syndromes
  • Imd2
  • Immunodeficiency 2
  • Immunodeficiency 2s
  • Aldrich Syndrome
  • Eczema-Thrombocytopenia-Immunodeficiency Syndrome
  • Eczema Thrombocytopenia Immunodeficiency Syndrome
  • Eczema-Thrombocytopenia-Immunodeficiency Syndromes

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