"Mucopolysaccharidoses" 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.
Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency.
| Descriptor ID |
D009083
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| MeSH Number(s) |
C16.320.565.202.715 C16.320.565.595.600 C17.300.550.575 C18.452.648.202.715 C18.452.648.595.600
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Mucopolysaccharidoses".
Below are MeSH descriptors whose meaning is more specific than "Mucopolysaccharidoses".
This graph shows the total number of publications written about "Mucopolysaccharidoses" by people in this website by year, and whether "Mucopolysaccharidoses" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
| 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Mucopolysaccharidoses" by people in Profiles.
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MPSBase: Comprehensive repository of differentially expressed genes for mucopolysaccharidoses. Mol Genet Metab. 2021 08; 133(4):372-377.
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The lysosomal disease caused by mutant VPS33A. Hum Mol Genet. 2019 08 01; 28(15):2514-2530.
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Mucopolysaccharidoses: anesthetic considerations and clinical manifestations. Middle East J Anaesthesiol. 2011 Jun; 21(2):243-50.
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Mucopolysaccharidosis presenting as pediatric multiple aortic aneurysm: first reported case. J Vasc Surg. 1997 Oct; 26(4):704-10.
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[Diagnosis and classification of mucopolysaccharidoses using the 35S-sulfate incorporation test]. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1986 Jun; 8(3):226-9.
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Diagnosis and classification of mucopolysaccharidoses using 35S-sulfate incorporation. Proc Chin Acad Med Sci Peking Union Med Coll. 1986; 1(2):116-9.
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[Laboratory diagnosis of lysosomal storage disease (glycoproteinosis Pompe's disease and Gaucher disease)]. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1985 Dec; 7(6):475-7.
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Mucopolysaccharidosis III B: hybridization studies on fibroblasts from a mild case and fibroblasts from severe patients. Clin Genet. 1984 Feb; 25(2):191-5.
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Deficiencies of glucosamine-6-sulfate or galactosamine-6-sulfate sulfatases are responsible for different mucopolysaccharidoses. Science. 1978 Jan 06; 199(4324):79-81.
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Mucopolysaccharidosis VI (Maroteaux-Lamy disease). Clinical and biochemical study of a mild variant case. Johns Hopkins Med J. 1974 Jul; 135(1):42-54.