An investigation of the possible influence of neutral alpha-glucosidases on the clinical heterogeneity of glycogenosis type II

Ann Hum Genet. 1989 May;53(2):185-92. doi: 10.1111/j.1469-1809.1989.tb01783.x.

Abstract

The lysosomal storage disorder glycogenosis type II, caused by a deficiency of lysosomal alpha-glucosidase, is very heterogeneous in its clinical presentation. It has been suggested that this heterogeneity may be due to differential expression of neutral alpha-glucosidases. We have therefore analysed the activity of the major neutral alpha-glucosidases in cultured fibroblasts or muscle cells from 26 patients with glycogenosis type II. The results indicate that there is no correlation between the expression of neutral alpha-glucosidase isoenzymes and the clinical phenotype of this disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • Electrophoresis, Cellulose Acetate
  • Electrophoresis, Starch Gel
  • Fibroblasts
  • Glycogen Storage Disease Type II / enzymology
  • Glycogen Storage Disease Type II / genetics*
  • Humans
  • Lysosomes / enzymology
  • Muscles / metabolism
  • Phenotype
  • alpha-Glucosidases / deficiency
  • alpha-Glucosidases / genetics*
  • alpha-Glucosidases / metabolism

Substances

  • alpha-Glucosidases