Literature DB >> 523191

Multiple deficiency of mucopolysaccharide sulfatases in mucosulfatidosis.

R Basner, K von Figura, J Glössl, U Klein, H Kresse, W Mlekusch.   

Abstract

Fibroblasts of four patients affected with mucosulfatidosis (multiple sulfatase deficiency, Austin variant of metachromatic leukodystrophy) were assayed for activities of the five sulfatases known to degrade mucopolysaccharides. These were iduronide 2-sulfate sulfatase, sulfamidase, N-acetyl-galactosamine 6-sulfate sulfatase, arylsulfatase B (N-acetylgalactosamine 4-sulfate sulfatase), and N-acetylglucosamine 6-sulfate sulfatase. The activities of these five sulfatases were severely depressed, thus confirming the known deficiency of arylsulfatase B and the absence of the Hunter and Sanfilippo III A corrective factors that have iduronide 2-sulfate sulfatase and sulfamidase activity, respectively. Together with earlier reports of the deficiencies of arylsulfatases A and C, cholesteryl sulfatase, and dehydroepiandrosterone sulfatae, mucosulfatidosis is now characterized by the deficiency of nine different sulfatases.

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Year:  1979        PMID: 523191     DOI: 10.1203/00006450-197912000-00002

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  12 in total

Review 1.  Metabolic syndromes with dermatologic manifestations.

Authors:  M Irons; H L Levy
Journal:  Clin Rev Allergy       Date:  1986-02

2.  Multiple sulphatase deficiency with early onset.

Authors:  E Vamos; I Liebaers; N Bousard; J Libert; N Perlmutter
Journal:  J Inherit Metab Dis       Date:  1981       Impact factor: 4.982

3.  Mammalian arylsulfatases A and B: relative rates of hydrolysis of artificial substrates.

Authors:  D B Thompson; W L Daniel
Journal:  Experientia       Date:  1986-02-15

4.  The mucopolysaccharidoses: biochemistry and clinical symptoms.

Authors:  H Kresse; M Cantz; K von Figura; J Glössl; E Paschke
Journal:  Klin Wochenschr       Date:  1981-08-17

5.  Multiple sulfatase deficiency (mucosulfatidosis): impaired degradation of labeled sulfated compounds in cultured skin fibroblasts in vivo.

Authors:  Y Eto; S Numaguchi; T Tahara; O M Rennert
Journal:  Eur J Pediatr       Date:  1980-10       Impact factor: 3.183

6.  Biochemical variability of arylsulphatases -A, -B and -C in cultured fibroblasts from patients with multiple sulphatase deficiency.

Authors:  P L Chang; N E Rosa; S R Ballantyne; R G Davidson
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

7.  Complementation of multiple sulfatase deficiency in somatic cell hybrids.

Authors:  K Fedde; A L Horwitz
Journal:  Am J Hum Genet       Date:  1984-05       Impact factor: 11.025

8.  Immunofluorescence staining and immunological studies of arylsulphatase A of multiple sulphatase deficiency (MSD) and metachromatic leukodystrophy (MLD) fibroblasts.

Authors:  A Tanaka; S Higami; G Isshiki; T Matsumoto; M Furusawa
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

9.  Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts.

Authors:  P L Chang; R G Davidson
Journal:  Proc Natl Acad Sci U S A       Date:  1980-10       Impact factor: 11.205

10.  Sanfilippo disease type D: deficiency of N-acetylglucosamine-6-sulfate sulfatase required for heparan sulfate degradation.

Authors:  H Kresse; E Paschke; K von Figura; W Gilberg; W Fuchs
Journal:  Proc Natl Acad Sci U S A       Date:  1980-11       Impact factor: 11.205

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