Glycogen metabolism disorder that has material basis in enzymes deficiencies necessary in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types.
A 17-yr-old female received a liver transplant for type I glycogenstoragedisease.
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The recipient was a 2-year-old girl affected by glycogenstoragedisease type IV.
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A boy with marked hepatomegaly and motor weakness was investigated for glycogenstoragedisease.
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Patients with glycogenstoragedisease (GSD) type IA were not excluded.
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Any lesions that were suspected of neurogenic atrophy, traumatic muscular degeneration, glycogenstoragedisease or other porcine muscular disorders were not observed.
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Glycogenstoragedisease type IX (GSD type IX) results from a deficiency of hepatic phosphorylase kinase activity.
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Glycogenstoragediseases (GSD) are inherited metabolic disorders of glycogen metabolism due to intracellular enzyme deficiency resulting in abnormal storage of glycogen in tissues.