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