"Mucopolysaccharidosis IV" 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.
Genetic disorder of mucopolysaccharide metabolism characterized by skeletal abnormalities, joint instability, development of cervical myelopathy, and excessive urinary keratan sulfate. There are two biochemically distinct forms, each due to a deficiency of a different enzyme.
Descriptor ID |
D009085
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MeSH Number(s) |
C16.320.565.202.715.655 C16.320.565.595.600.655 C17.300.550.575.655 C18.452.648.202.715.655 C18.452.648.595.600.655
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Concept/Terms |
Mucopolysaccharidosis IV- Mucopolysaccharidosis IV
- Eccentroosteochondrodysplasia
- Eccentroosteochondrodysplasias
- Morquio Disease
- Disease, Morquio
- Mucopolysaccharidosis Type IV
- IV, Mucopolysaccharidosis Type
- IVs, Mucopolysaccharidosis Type
- Mucopolysaccharidosis Type IVs
- Type IV, Mucopolysaccharidosis
- Type IVs, Mucopolysaccharidosis
- Morquio's Disease
- Disease, Morquio's
- Morquios Disease
- Morquio's Syndrome
- Morquios Syndrome
- Syndrome, Morquio's
- Mucopolysaccharidosis 4
- Eccentro-Osteochondrodysplasia
- Eccentro Osteochondrodysplasia
- Eccentro-Osteochondrodysplasias
- Morquio Syndrome
- Morquio Syndromes
- Syndrome, Morquio
- Syndromes, Morquio
Mucopolysaccharidosis Type IV A- Mucopolysaccharidosis Type IV A
- Morquio A Disease
- Disease, Morquio A
- Mucopolysaccharidosis Type IVA
- MPS IV A
- MPS IVA
- Galactosamine-6-Sulfatase Deficiency
- Deficiencies, Galactosamine-6-Sulfatase
- Deficiency, Galactosamine-6-Sulfatase
- Galactosamine 6 Sulfatase Deficiency
- Galactosamine-6-Sulfatase Deficiencies
- Morquio Syndrome A
- Syndrome A, Morquio
Mucopolysaccharidosis Type IV B- Mucopolysaccharidosis Type IV B
- Morquio Syndrome B
- Morquio Syndrome, Type B
- Mucopolysaccharidosis Type IVB
- Mucopolysaccharidosis Type IVBs
- Morquio-B Disease
- Disease, Morquio-B
- Morquio B Disease
- MPS IV B
- MPS IVB
- Mucopolysaccharidosis 4B
- Mucopolysaccharidosis 4Bs
- Morquio B Syndrome
- Syndrome, Morquio B
- Morquio's Disease Type B
GALNS Deficiency- GALNS Deficiency
- Deficiencies, GALNS
- Deficiency, GALNS
- GALNS Deficiencies
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Below are MeSH descriptors whose meaning is more general than "Mucopolysaccharidosis IV".
Below are MeSH descriptors whose meaning is more specific than "Mucopolysaccharidosis IV".
This graph shows the total number of publications written about "Mucopolysaccharidosis IV" by people in this website by year, and whether "Mucopolysaccharidosis IV" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2015 | 1 | 0 | 1 |
2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Mucopolysaccharidosis IV" by people in Profiles.
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Successful Elosulfase Alfa Desensitization Protocol in a Patient With Morquio A Syndrome. Pediatrics. 2022 02 01; 149(2).
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Safety and physiological effects of two different doses of elosulfase alfa in patients with morquio a syndrome: A randomized, double-blind, pilot study. Am J Med Genet A. 2015 Oct; 167A(10):2272-81.
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The mouse N-acetylgalactosamine-6-sulfate sulfatase (Galns) gene: cDNA isolation, genomic characterization, chromosomal assignment and analysis of the 5'-flanking region. Biochim Biophys Acta. 2000 Mar 17; 1500(3):323-34.
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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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Deficiencies of glucosamine-6-sulfate or galactosamine-6-sulfate sulfatases are responsible for different mucopolysaccharidoses. Science. 1978 Jan 06; 199(4324):79-81.