Pediatric glycogen storage disease type III

Glycogen storage disease (GSD) is an autosomal recessive genetic disease, a class of disorders of glycogen metabolism caused by defects in innate enzymes (debranching enzymes). Glycogen storagy disease type Ⅲ (Glycogen storagy disease type Ⅲ), also known as Cori Ⅲ type glycogen storage syndrome, also known as Cori disease, debranching enzyme deficiency, Forbes disease, limited dextrinosis, debranching Enzymes Debrancher glycogen storage disease, Forbes syndrome, etc. Liver damage is most severe in this disease.

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