[Natural history of hepatic glycogen storage diseases]

Presse Med. 2008 Jul-Aug;37(7-8):1172-7. doi: 10.1016/j.lpm.2007.09.023. Epub 2008 Feb 29.
[Article in French]

Abstract

Hepatic glycogen storage diseases are rare inherited conditions affecting glycogen metabolism. During the last twenty years, medical progress has allowed children who used to die before they reached the age of ten years to reach adulthood. It is important to know the natural history and long-term outcome of these patients to improve their treatment during childhood. To reach this goal, collaboration between pediatric specialists and those who treat adults is essential.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Glycogen Storage Disease Type I / diagnosis
  • Glycogen Storage Disease Type I / physiopathology*
  • Glycogen Storage Disease Type I / therapy
  • Glycogen Storage Disease Type III / diagnosis
  • Glycogen Storage Disease Type III / physiopathology
  • Glycogen Storage Disease Type III / therapy
  • Glycogen Storage Disease Type IV / diagnosis
  • Glycogen Storage Disease Type IV / physiopathology
  • Glycogen Storage Disease Type IV / therapy
  • Growth
  • Humans
  • Liver Diseases / diagnosis
  • Liver Diseases / physiopathology
  • Liver Diseases / therapy
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / physiopathology
  • Treatment Outcome