Glucose-6-phosphatase gene mutations in Taiwan Chinese patients with glycogen storage disease type Ia

J Hum Genet. 2000;45(4):197-9. doi: 10.1007/s100380070026.

Abstract

Glycogen storage disease type Ia (GSD Ia) is caused by a deficiency of glucose-6-phosphatase (G6Pase) activity. Eighteen GSD Ia families were studied for G6Pase gene mutations. Thirty-two mutations were found in 36 GSD Ia chromosomes: 16 were 727 G-->T (44.44%); 13 were R83H (327 G-->T; 36.11%); 1 was 341delG; 1 was 933insAA; and 1 was 793 G-->T. The 727 G-->T and R83H mutations together accounted for 80.56% (29/36) of the GSD Ia chromosomes. These two mutations were easily examined by polymerase chain reaction-based methods, and the prenatal diagnosis of a non-affected fetus was successfully made. The 727 G-->T mutation is the predominant mutation in Japanese GSD Ia patients, but is rarely seen in Western counties. The 727 G-->T mutation is also the most prevalent mutation in Taiwan Chinese, although the incidence is not as high as in Japan.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asian People
  • Child
  • Child, Preschool
  • Chorionic Villi Sampling
  • DNA / blood
  • Female
  • Frameshift Mutation
  • Genetic Testing
  • Glucose-6-Phosphatase / genetics*
  • Glucose-6-Phosphatase / metabolism
  • Glycogen Storage Disease Type I / genetics*
  • Haplotypes
  • Humans
  • Infant
  • Male
  • Point Mutation
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length
  • Pregnancy
  • Taiwan

Substances

  • DNA
  • Glucose-6-Phosphatase