Glycogen storage disease due to liver glycogen synthase deficiency (Q100829): Difference between revisions
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Revision as of 17:36, 16 August 2026
Hepatic glycogen synthase deficiency, or glycogen storage disease (GSD) type 0, is a genetically inherited anomaly of glycogen metabolism and a form of GSD characterised by fasting hypoglycaemia. This is not a glycogenosis, strictly speaking, as the enzyme deficiency decreases glycogen reserves. Patients present with morning fatigue and fasting hypoglycaemia (without hepatomegaly) associated with hyperketonemia but without hyperalaninemia or hyperlactacidemia. After meals, major hyperglycemia associated with lactate and alanine increase and hyperlipidemia is observed.
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| default for all languages | ID_1927530758 |
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| English | Glycogen storage disease due to liver glycogen synthase deficiency |
Hepatic glycogen synthase deficiency, or glycogen storage disease (GSD) type 0, is a genetically inherited anomaly of glycogen metabolism and a form of GSD characterised by fasting hypoglycaemia. This is not a glycogenosis, strictly speaking, as the enzyme deficiency decreases glycogen reserves. Patients present with morning fatigue and fasting hypoglycaemia (without hepatomegaly) associated with hyperketonemia but without hyperalaninemia or hyperlactacidemia. After meals, major hyperglycemia associated with lactate and alanine increase and hyperlipidemia is observed. |
