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Concept information

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

Terme préférentiel

Wiskott-Aldrich Syndrome  

Type

  • mesh:Descriptor

Définition

  • 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.

Concept générique

Synonyme(s)

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

Qualificatif(s) autorisé(s)

Traductions

  • Syndrome de Wiskott-Aldrich

    français

  • 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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RDF/XML TURTLE JSON-LD Date de création 01/01/1999, dernière modification le 17/06/2019