 Mucopolysaccharidosis VI
"Mucopolysaccharidosis VI" 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.
Mucopolysaccharidosis with excessive CHONDROITIN SULFATE B in urine, characterized by dwarfism and deafness. It is caused by a deficiency of N-ACETYLGALACTOSAMINE-4-SULFATASE (arylsulfatase B).
| Descriptor ID |
D009087
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| MeSH Number(s) |
C16.320.565.202.715.670 C16.320.565.595.600.670 C17.300.550.575.670 C18.452.648.202.715.670 C18.452.648.595.600.670
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| Concept/Terms |
Mucopolysaccharidosis VI- Mucopolysaccharidosis VI
- Arylsulfatase B Deficiency
- Arylsulfatase B Deficiencies
- Deficiencies, Arylsulfatase B
- Deficiency, Arylsulfatase B
- Maroteaux-Lamy Syndrome
- Maroteaux Lamy Syndrome
- Syndrome, Maroteaux-Lamy
- Mucopolysaccharidosis Type VI
- Type VI, Mucopolysaccharidosis
- Mucopolysaccharidosis Type 6
- Type 6, Mucopolysaccharidosis
- N-Acetylgalactosamine-4-Sulfatase Deficiency
- Deficiencies, N-Acetylgalactosamine-4-Sulfatase
- Deficiency, N-Acetylgalactosamine-4-Sulfatase
- N-Acetylgalactosamine-4-Sulfatase Deficiencies
- Polydystrophic Dwarfism
- Dwarfism, Polydystrophic
- ARSB Deficiency
- ARSB Deficiencies
- Deficiencies, ARSB
- Deficiency, ARSB
- Mucopolysaccharidosis 6
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Below are MeSH descriptors whose meaning is more general than "Mucopolysaccharidosis VI".
Below are MeSH descriptors whose meaning is more specific than "Mucopolysaccharidosis VI".
This graph shows the total number of publications written about "Mucopolysaccharidosis VI" by people in this website by year, and whether "Mucopolysaccharidosis VI" 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 |
|---|
| 2012 | 1 | 0 | 1 | | 2014 | 1 | 0 | 1 | | 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Mucopolysaccharidosis VI" 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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Lachman RS, Burton BK, Clarke LA, Hoffinger S, Ikegawa S, Jin DK, Kano H, Kim OH, Lampe C, Mendelsohn NJ, Shediac R, Tanpaiboon P, White KK. Mucopolysaccharidosis IVA (Morquio A syndrome) and VI (Maroteaux-Lamy syndrome): under-recognized and challenging to diagnose. Skeletal Radiol. 2014 Mar; 43(3):359-69.
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Solanki GA, Alden TD, Burton BK, Giugliani R, Horovitz DD, Jones SA, Lampe C, Martin KW, Ryan ME, Schaefer MK, Siddiqui A, White KK, Harmatz P. A multinational, multidisciplinary consensus for the diagnosis and management of spinal cord compression among patients with mucopolysaccharidosis VI. Mol Genet Metab. 2012 Sep; 107(1-2):15-24.
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