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Glycogen storage disease kind II, also called Pompe disease, and previously often called GSD-IIa. It’s brought on by an accumulation of glycogen in the lysosome attributable to deficiency of the lysosomal acid alpha-glucosidase enzyme. GSD-II and Danon illness are the only glycogen storage diseases with a defect in lysosomal metabolism, and Pompe disease was the […]