Glycogen storage disease type I: Diagnosis and phenotype/genotype correlation


Conference Paper

Glycogen storage disease type Ia (GSD Ia) is caused by mutations in the G6PC gene encoding the phosphatase of the microsomal glucose-6-phosphatase system. GSD Ia is characterized by hepatomegaly, hypoglycemia, lactic acidemia, hyperuricemia, hyperlipidemia and short stature. Other forms of GSD I (GSD I non-a) are characterized by the additional symptom of frequent infections caused by neutropenia and neutrophil dysfunction. GSD I non-a is caused by mutations in a gene encoding glucose-6-phosphatase translocase (G6PT1). We report on the molecular genetic analyses of G6PC and G6PT1 in 130 GSD Ia patients and 15 GSD I non-a patients, respectively, and provide an overview of the current literature pertaining to the molecular genetics of GSD I. Among the GSD Ia patients, 34 different mutations were identified, two of which have not been described before (A65P; F177C). Seventeen different mutations were detected in the GSD I non-a patients. True common mutations were identified neither in GSD Ia nor in GSD I non-a patients. Conclusion: Glycogen storage disease type Ia and and type I non-a are genetically heterogenous disorders. For the diagnosis of the various forms of glycogen storage disease type I, molecular genetic analyses are reliable and convenient alternatives to the enzyme assays in liver biopsy specimens. Some genotype-phenotype correlations exist, for example, homozygosity for one G6PC mutation, G188R, seems to be associated with a glycogen storage disease type I non-a phenotype and homozygosity for the 727G > T mutation may be associated with a milder phenotype but an increased risk for hepatocellular carcinoma. © Springer-Verlag 2002.

Full Text

Duke Authors

Cited Authors

  • Matern, D; Seydewitz, HH; Bali, D; Lang, C; Chen, YT

Published Date

  • January 1, 2002

Published In

Volume / Issue

  • 161 / 1

Start / End Page

  • S10 - S19

International Standard Serial Number (ISSN)

  • 0943-9676

Digital Object Identifier (DOI)

  • 10.1007/bf02679989

Citation Source

  • Scopus