language-icon Old Web
English
Sign In

Glycogen storage disease

A glycogen storage disease (GSD, also glycogenosis and dextrinosis) is a metabolic disorder caused by enzyme deficiencies affecting either glycogen synthesis, glycogen breakdown or glycolysis (glucose breakdown), typically within muscles and/or liver cells.(PGAM2) A glycogen storage disease (GSD, also glycogenosis and dextrinosis) is a metabolic disorder caused by enzyme deficiencies affecting either glycogen synthesis, glycogen breakdown or glycolysis (glucose breakdown), typically within muscles and/or liver cells. GSD has two classes of cause: genetic and acquired. Genetic GSD is caused by any inborn error of metabolism (genetically defective enzymes) involved in these processes. In livestock, acquired GSD is caused by intoxication with the alkaloid castanospermine.

[ "Glycogen", "Disease", "Debrancher enzyme", "Glycogen storage disease type Ia", "Hepatic glycogen storage", "Glucose-6-phosphate translocase", "Phosphorylase B Kinase Deficiency" ]
Parent Topic
Child Topic
    No Parent Topic