Literature DB >> 2964538

Urinary screening for disorders of heteroglycan metabolism. Results of 10 years experience with a comprehensive system.

A C Sewell1.   

Abstract

The results of 10 years experience in urinary screening for disorders of heteroglycan metabolism are presented. Over 5,000 urines were analysed of which 216 were positive for excess mucopolysacchariduria. The enzymatic diagnosis was achieved in 159 mucopolysaccharidoses of which Type III Sanfilippo was the commonest (86 cases), followed by Type II Hunter (31 cases) and Type I Hurler (21 cases). A total of 27 urines were positive for excess oligosacchariduria, the enzymatic diagnosis being established in 20 cases. The most frequently encountered oligosaccharidosis was GM1 gangliosidosis (10 cases), followed by mannosidosis (5 cases). No cases of fucosidosis were found.

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Year:  1988        PMID: 2964538     DOI: 10.1007/bf01713010

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN: 0023-2173


  24 in total

1.  Simple spectrophotometric quantification of urinary excretion of glycosaminoglycan sulfates.

Authors:  G Panin; S Naia; R Dall'Amico; L Chiandetti; F Zachello; C Catassi; L Felici; G V Coppa
Journal:  Clin Chem       Date:  1986-11       Impact factor: 8.327

2.  A review and selection of simple laboratory methods used for the study of glycosaminoglycan excretion and the diagnosis of the mucopolysaccharidoses.

Authors:  C A Pennock
Journal:  J Clin Pathol       Date:  1976-02       Impact factor: 3.411

3.  Structural determination of three glycoasparagines isolated from the urine of a patient with aspartylglycosaminuria.

Authors:  A Lundblad; P K Masson; N E Nordén
Journal:  Eur J Biochem       Date:  1976-08-01

4.  Structure of nine sialyl-oligosaccharides accumulated in urine of eleven patients with three different types of sialidosis. Mucolipidosis II and two new types of mucolipidosis.

Authors:  G Strecker; M C Peers; J C Michalski; T Hondi-Assah; B Fournet; G Spik; J Montreuil; J P Farriaux; P Maroteaux; P Durand
Journal:  Eur J Biochem       Date:  1977-05-16

5.  Biochemical definition of the mucopolysaccharidoses.

Authors:  J W Spranger
Journal:  Z Kinderheilkd       Date:  1970

6.  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

7.  The quantitative measurement of Alcian Blue-glycosaminoglycan complexes.

Authors:  P Whiteman
Journal:  Biochem J       Date:  1973-02       Impact factor: 3.857

8.  [Phenotypes in heteroglycanoses and sphingolipidoses (author's transl)].

Authors:  J Gehler
Journal:  Monatsschr Kinderheilkd       Date:  1981-11       Impact factor: 0.323

9.  Mucopolysaccharidosis type VII (beta-glucuronidase deficiency): a report of a new case and a survey of those in the literature.

Authors:  A C Sewell; J Gehler; G Mittermaier; E Meyer
Journal:  Clin Genet       Date:  1982-06       Impact factor: 4.438

10.  Structure of seven oligosaccharides excreted in the urine of a patient with Sandhoff's disease (GM2 gangliosidosis-variant O).

Authors:  G Strecker; M C Herlant-Peers; B Fournet; J Montreul
Journal:  Eur J Biochem       Date:  1977-11-15
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  2 in total

1.  Diagnosis of mucopolysaccharidoses: how to avoid false positives and false negatives.

Authors:  K Mahalingam; S Janani; S Priya; E M Elango; R Maya Sundari
Journal:  Indian J Pediatr       Date:  2004-01       Impact factor: 1.967

2.  Epidemiology of Sanfilippo syndrome: results of a systematic literature review.

Authors:  Tamás Zelei; Kata Csetneki; Zoltán Vokó; Csaba Siffel
Journal:  Orphanet J Rare Dis       Date:  2018-04-10       Impact factor: 4.123

  2 in total

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