TY - CHAP M1 - Book, Section TI - Glycogen Storage Diseases (GSD): An Overview A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/03 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164070963 ER -