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Hemic and Lymphatic Diseases > Hematologic Diseases > Hemorrhagic Disorders > Wiskott-Aldrich Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Blood Coagulation Disorders, Inherited > Wiskott-Aldrich Syndrome
Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Coagulation Disorders > Blood Coagulation Disorders, Inherited > Wiskott-Aldrich Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Primary Immunodeficiency Diseases > Wiskott-Aldrich Syndrome
Immune System Diseases > Immunologic Deficiency Syndromes > Primary Immunodeficiency Diseases > Wiskott-Aldrich Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Genetic Diseases, X-Linked > Wiskott-Aldrich Syndrome
Immune System Diseases > Immunologic Deficiency Syndromes > Lymphopenia > Wiskott-Aldrich Syndrome
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Leukocyte Disorders > Leukopenia > Lymphopenia > Wiskott-Aldrich Syndrome

Preferred term

Wiskott-Aldrich Syndrome  

Type

  • mesh:Descriptor

Definition

  • 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.

Broader concept

Entry terms

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

Allowable Qualifier(s)

In other languages

  • Syndrome de Wiskott-Aldrich

    French

  • Eczéma-thrombocytopénie-immunodéficience
  • Maladie de Wiskott-Aldrich
  • Syndrome d'Aldrich
  • WAS (Wiskott-Aldrich Syndrome)

URI

http://data.loterre.fr/ark:/67375/JVR-MVS1D7T9-J

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