 Mucopolysaccharidoses
"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
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| Concept/Terms |
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 1 | 0 | 1 | | 2013 | 1 | 0 | 1 | | 2014 | 1 | 0 | 1 | | 2017 | 0 | 1 | 1 | | 2018 | 1 | 0 | 1 | | 2021 | 1 | 0 | 1 | | 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Mucopolysaccharidoses" by people in Profiles.
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Miller BS, Fung EB, White KK, Lund TC, Harmatz P, Orchard PJ, Whitley CB, Polgreen LE. Persistent bone and joint disease despite current treatments for mucopolysaccharidosis types I, II, and VI: Data from a 10-year prospective study. J Inherit Metab Dis. 2023 07; 46(4):695-704.
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Georgiadis AG, Koester TM, Mackenzie WG, Nahm NJ, Novotny SA, Rogers KJ, Siljander BR, Sousa TC, White KK, Walker KR. Intraoperative Neurological Monitoring in Lower Limb Surgery for Patients With Mucopolysaccharidoses. J Pediatr Orthop. 2021 Mar 01; 41(3):182-189.
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Ghotme KA, Alvarado-Gomez F, Lampe C, White KK, Solano-Villareal M, Giugliani R, Harmatz PR. Spinal cord issues in adult patients with MPS: transition of care survey. Childs Nerv Syst. 2018 09; 34(9):1759-1765.
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White KK. Carpal tunnel syndrome in mucopolysaccharidosis: the value of rare disease registries. Dev Med Child Neurol. 2017 12; 59(12):1213-1214.
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O'Brien A, Bompadre V, Hale S, White KK. Musculoskeletal function in patients with mucopolysaccharidosis using the pediatric outcomes data collection instrument. J Pediatr Orthop. 2014 Sep; 34(6):650-4.
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White KK, Sousa T. Mucopolysaccharide disorders in orthopaedic surgery. J Am Acad Orthop Surg. 2013 Jan; 21(1):12-22.
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White KK. Orthopaedic aspects of mucopolysaccharidoses. Rheumatology (Oxford). 2011 Dec; 50 Suppl 5:v26-33.
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