Literature DB >> 2941619

Possible prenatal diagnosis of type III glycogenosis.

I Maire, M Mathieu.   

Abstract

This paper reports the first prenatal diagnosis in a pregnancy at risk for type III glycogenosis using a reliable test for amylo-1,6-glucosidase in cultured amniotic fluid cells. This test, based upon the different rates of glycogen and phosphorylase limit dextrin hydrolysis, was found to be more reliable in detecting a deficiency of amylo-1,6-glucosidase activity than either phosphorylase limit dextrin hydrolysis alone or [14C]glucose incorporation using leukocytes and cultured cells.

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Year:  1986        PMID: 2941619     DOI: 10.1007/bf01813908

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  2 in total

1.  The apparent activity in vivo of the lysosomal pathway of glycogen catabolism in cultured human skin fibroblasts from patients with type III glycogen storage disease.

Authors:  D H Brown; L M Waindle; B I Brown
Journal:  J Biol Chem       Date:  1978-07-25       Impact factor: 5.157

2.  Incorporation of [14C]glucose into alpha-1,4 bonds of glycogen by leukocytes and fibroblasts of patients with type III glycogen storage disease.

Authors:  A Gutman; V Barash; H Schramm; R J Deckelbaum; E Granot; M Aker; G Kohn
Journal:  Pediatr Res       Date:  1985-01       Impact factor: 3.756

  2 in total
  2 in total

Review 1.  Prenatal diagnosis of enzyme defects.

Authors:  B Winchester
Journal:  Arch Dis Child       Date:  1990-01       Impact factor: 3.791

2.  First trimester prenatal diagnosis of glycogen storage disease type III.

Authors:  I Maire; G Mandon; M Mathieu
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

  2 in total

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