RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164070963 T1 Glycogen Storage Diseases (GSD): An Overview T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164070963 RD 2024/10/08 AB There are fifteen distinct glycogen storage diseases. Although glycogen synthase deficiency does not result in storage of extra glycogen in the liver, it is usually classified with the GSD Type 0 because it is another defect of glycogen storage and can cause similar problems. The overall frequency of glycogen-storage disease has been established approximately 1:20,000 to 25,000 people worldwide.