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[Natural history of hepatic glycogen storage diseases]

Authors :
Philippe, Labrune
Pascale Trioche, Eberschweiler
Alix Mollet, Boudjemline
Aurélie, Hubert-Buron
François, Petit
Vincent, Gajdos
Source :
Presse medicale (Paris, France : 1983). 37(7-8)
Publication Year :
2007

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.

Details

Language :
French
ISSN :
22130276
Volume :
37
Issue :
7-8
Database :
OpenAIRE
Journal :
Presse medicale (Paris, France : 1983)
Accession number :
edsair.pmid..........445228fb88c195d490e4849339ba9f7f