Case Report: Liver Glycogen Synthase Deficiency—A Cause of Ketotic Hypoglycemia

Author:

Rutledge S. Lane1,Atchison Joycelyn2,Bosshard Nils U.,Steinmann Beat

Affiliation:

1. Division of Neurology

2. Division of Endocrinology

Abstract

Glycogen synthase deficiency is a rare inborn error of metabolism, characterized by fasting hypoglycemia, hypoglycemic seizures, and ketonuria. Only 7 families with 14 affected children have been reported. Here, we report an additional patient with this deficiency. Findings in this patient were clinically and biochemically consistent with those reported in patients with ketotic hypoglycemia and may alert the clinician to consider glycogen synthase deficiency.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

Reference11 articles.

1. Infantile hypoglycaemia due to inherited deficiency of glycogen synthetase in liver.;Lewis;Arch Dis Child,1963

2. Hepatic Glycogen Synthetase Deficiency: Further Studies on a Family

3. Hepatic glycogen synthetase deficiency.;Aynsley-Green;Arch Dis Child,1977

4. Asymptomatic hepatic glycogen-synthetase deficiency.;Aynsley-Green;Lancet,1978

5. Deficiencia en glucogeno sintetasa hepatica o glucogenosis tipo cero.;De Kremer;Medicina (Buenos Aires),1990

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