"Wiskott-Aldrich Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D014923
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| MeSH 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
|
| Concept/Terms |
Wiskott-Aldrich Syndrome- Wiskott-Aldrich Syndrome
- 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
|
Below are MeSH descriptors whose meaning is more general than "Wiskott-Aldrich Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Wiskott-Aldrich Syndrome".
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Below are the most recent publications written about "Wiskott-Aldrich Syndrome" by people in Profiles.