Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Preferred term
Wiskott-Aldrich Syndrome
Type
-
Topical Descriptor
Broader concept
Entry terms
- Aldrich Syndrome
- Eczema Thrombocytopenia Immunodeficiency Syndrome
- Eczema-Thrombocytopenia-Immunodeficiency Syndrome
- Eczema-Thrombocytopenia-Immunodeficiency Syndromes
- Imd2
- Immunodeficiency 2
- Immunodeficiency 2s
- Wiskott Syndrome
- Wiskott Syndromes
Scope note
- 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.
History note
- 85; was ALDRICH SYNDROME 1963-84
In other languages
-
Finnish
-
Aldrich
-
deficientia immunalis cum thrombocytopenia et eczemate
-
immunbrist med trombocytopeni och eksem
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immuunivajavuus ja trombosytopenia ja ekseema
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syndroma Wiskott-Aldrich
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Wiskott
-
Wiskott-Aldrich
-
Wiskott-Aldrichin syndrooma
-
Swedish
URI
http://www.yso.fi/onto/mesh/D014923
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