Literature DB >> 1838126

Apparent absence of glycogen branching enzyme activity in phosphofructokinase deficiency.

V Barash1, S Lilling, R Fischer, Z Argov.   

Abstract

A 30-year-old woman with clinical features and biochemical findings of muscle phosphofructokinase deficiency was found to have a very low level of alpha-1,4-glucan:alpha-1,4-glucan-6-transglucosylase (branching enzyme, EC 2.4.1.18) activity in muscle. In contrast, branching enzyme activity in the leukocytes was in the range of control values. After sedimentation of the glycogen from muscle homogenates by centrifugation at 105,000 g, branching enzyme activity in muscle of the patient was similar to that of control subjects. This patient illustrates the possibility of falsely diagnosing branching enzyme deficiency when muscle glycogen content is elevated. It is likely that such an artefact may also cause a false positive diagnosis of branching enzyme deficiency in other metabolic diseases associated with glycogen accumulation.

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Year:  1991        PMID: 1838126     DOI: 10.1007/bf01800471

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


  6 in total

1.  PHOSPHOFRUCTOKINASE DEFICIENCY IN SKELETAL MUSCLE. A NEW TYPE OF GLYCOGENOSIS.

Authors:  S TARUI; G OKUNO; Y IKURA; T TANAKA; M SUDA; M NISHIKAWA
Journal:  Biochem Biophys Res Commun       Date:  1965-05-03       Impact factor: 3.575

2.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

3.  Lack of an alpha-1,4-glucan: alpha-1,4-glucan 6-glycosyl transferase in a case of type IV glycogenosis.

Authors:  B I Brown; D H Brown
Journal:  Proc Natl Acad Sci U S A       Date:  1966-08       Impact factor: 11.205

4.  Purification and subunit structure of glycogen-branching enzyme from rabbit skeletal muscle.

Authors:  F B Caudwell; P Cohen
Journal:  Eur J Biochem       Date:  1980-08

5.  A new variant of type IV glycogenosis: deficiency of branching enzyme activity without apparent progressive liver disease.

Authors:  H L Greene; B I Brown; D T McClenathan; R M Agostini; S R Taylor
Journal:  Hepatology       Date:  1988 Mar-Apr       Impact factor: 17.425

6.  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

  6 in total
  1 in total

1.  Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder.

Authors:  Sing-Chung Li; Chiao-Ming Chen; Jennifer L Goldstein; Jer-Yuarn Wu; Emmanuelle Lemyre; Thomas Andrew Burrow; Peter B Kang; Yuan-Tsong Chen; Deeksha S Bali
Journal:  J Inherit Metab Dis       Date:  2010-01-08       Impact factor: 4.982

  1 in total

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