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This document provides information about Glycogen Storage Disease (GSD), including the seven main types defined by the enzyme deficiency, symptoms, inheritance patterns, and treatment approaches. GSD results from the buildup of glycogen in the body due to missing or non-functioning enzymes involved in glycogen breakdown. Symptoms vary by type but often include poor growth, muscle cramps, low blood sugar, enlarged liver, and abdominal swelling. Most types are inherited in an autosomal recessive pattern, thou

Author

Cha Canceran

Language

EN