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Up to: Disorder of glycogen metabolism

Glycogen storage disorder due to hepatic glycogen synthase deficiency

Glycogen synthetase deficiency, or glycogen storage disease (GSD) type 0, is a genetically inherited anomaly of glycogen metabolism and a form of GSD characterized by fasting hypoglycemia. This is not a glycogenosis, strictly speaking, as the enzyme deficiency decreases glycogen reserves.

2 trials tagged with this condition →

This condition has no sub-types.