 Wiskott-Aldrich Syndrome
"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
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| 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
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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".
This graph shows the total number of publications written about "Wiskott-Aldrich Syndrome" by people in this website by year, and whether "Wiskott-Aldrich Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 2 | 1 | 3 | | 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Wiskott-Aldrich Syndrome" by people in Profiles.
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Gaikwad P, Bargir UA, Jodhawat N, Dalvi A, Shinde S, Tamhankar P, Setia P, Kambli P, Dhawale A, Temkar L, Vedpathak D, Jose A, Gupta M, Yadav-Malik R, Dutta S, Bose K, Taur P, Gowri V, Iyengar V, Chougule A, Desai M, Sivasankaran M, Bhattad S, Balaji S, Mudaliar S, Kacha A, Subramanian G, Patel S, Sharma S, Sampagar A, Madkaikar M. Mutational Landscape of Patients with Wiskott Aldrich Syndrome: Update from India. J Clin Immunol. 2024 Dec 17; 45(1):56.
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Chinen J, Anmuth D, Franklin AR, Shearer WT. Long-term follow-up of patients with primary immunodeficiencies. J Allergy Clin Immunol. 2007 Oct; 120(4):795-7.
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Majstoravich S, Zhang J, Nicholson-Dykstra S, Linder S, Friedrich W, Siminovitch KA, Higgs HN. Lymphocyte microvilli are dynamic, actin-dependent structures that do not require Wiskott-Aldrich syndrome protein (WASp) for their morphology. Blood. 2004 Sep 01; 104(5):1396-403.
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Chen XM, Huang BQ, Splinter PL, Orth JD, Billadeau DD, McNiven MA, LaRusso NF. Cdc42 and the actin-related protein/neural Wiskott-Aldrich syndrome protein network mediate cellular invasion by Cryptosporidium parvum. Infect Immun. 2004 May; 72(5):3011-21.
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Gismondi A, Cifaldi L, Mazza C, Giliani S, Parolini S, Morrone S, Jacobelli J, Bandiera E, Notarangelo L, Santoni A. Impaired natural and CD16-mediated NK cell cytotoxicity in patients with WAS and XLT: ability of IL-2 to correct NK cell functional defect. Blood. 2004 Jul 15; 104(2):436-43.
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Kirkpatrick CH. Restoration of cell-mediated immune responses with transfer factor. Birth Defects Orig Artic Ser. 1975; 11(1):441-4.
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