MPS IV - Morquio syndrome A

Stable Identifier
R-HSA-2206290
Type
Pathway
Species
Homo sapiens
ReviewStatus
5/5
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MPS IV - Morquio syndrome A
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Mucopolysaccharidosis IV A (MPS IVA, MPS4A, Morquio's syndrome, Morquio's; MIM:253000) is a rare, autosomal recessive mucopolysaccharide storage disease, first described simultaneously in 1929 by L Morquio (Morquio L, Sur une forme de distrophie familiale, Bull Soc Pediat, Paris, 27, 1929, 145-152) and JF Brailsford (Brailsford, JF, Chondro-osteo-dystrophy: roentgenographic and clinical features of child with dislocation of vertebrae, Am j Surg, 7, 1929, 404-410). MPSIVA is caused by a deficiency in N-acetylgalactosamine 6-sulfatase (GALNS; MIM:612222) which normally hydrolyses 6-sulfate groups of N-acetylgalactosamine 6-sulfate units of chondroitin sulfate (CS) and of galactose 6-sulfate units of keratan sulfate (KS) (Matalon et al. 1974). The result is accumulation of KS/DS in cells and overexcretion in urine. Severe osteochondrodysplasia is a commonly seen phenotype for this disease. The severity of the disease is variable but severe cases limits lifespan to their 20's or 30's (Prat et al. 2008, Tomatsu et al. 2011). The gene coding for human GALNS was mapped to chromosome 16q24.3 (Masuno et al. 1993) and its structure described at the same time by two independent groups as comprising 14 exons and spanning approximately 40-50 kb (Nakashima et al.1994, Morris et al.1994).
Literature References
PubMed ID Title Journal Year
8020961 Mucopolysaccharidosis IV A: molecular cloning of the human N-acetylgalactosamine-6-sulfatase gene (GALNS) and analysis of the 5'-flanking region

Shimozawa, N, Suzuki, Y, Fukuda, S, Sukegawa, K, Nakashima, Y, Orii, T, Kondo, N, Tomatsu, S, Hori, T

Genomics 1994
8001980 Morquio A syndrome: cloning, sequence, and structure of the human N-acetylgalactosamine 6-sulfatase (GALNS) gene

Apostolou, S, Guo, XH, Hopwood, JJ, Morris, CP, Scott, HS

Genomics 1994
4218100 Morquio's syndrome: deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfatase

Justice, P, Matalon, R, Arbogast, B, Dorfman, A, Brandt, IK

Biochem Biophys Res Commun 1974
18456538 Morquio syndrome: diagnosis in an adult

Prat, C, Zabraniecki, L, Bret, J, Lemaire, O, Fournié, B

Joint Bone Spine 2008
21506915 Mucopolysaccharidosis type IVA (Morquio A disease): clinical review and current treatment

Suzuki, Y, Thacker, MM, Chinen, Y, Barrera, L, Smith, M, Montaño, AM, Orii, T, Oikawa, H, Mackenzie, WG, Tomatsu, S

Curr Pharm Biotechnol 2011
8325655 Mucopolysaccharidosis IV A: assignment of the human N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene to chromosome 16q24

Masue, M, Fukuda, S, Sukegawa, K, Nakashima, Y, Orii, T, Masuno, M, Tomatsu, S, Hori, T

Genomics 1993
Participants
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Disease
Name Identifier Synonyms
mucopolysaccharidosis IV DOID:12804 mucopolysaccharidosis type IVA, Osteochondrodystrophy, deficiency of N-acetylgalactosamine-6-sulphatase, chondroosteodystrophy, Osteochondrodystrophy, Morquio syndrome A, MORQUIO A DISEASE, Mucopolysaccharidosis, MPS-IV-A (disorder), Mucopolysaccharidosis, MPS-IV, deficiency of chondroitinsulphatase, GALACTOSAMINE-6-SULFATASE DEFICIENCY
Authored
Jassal, B  (2012-04-26)
Reviewed
Coutinho, MF  (2012-08-27)
Alves, S  (2012-08-27)
Created
Jassal, B  (2012-04-26)
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