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Glycogen storage disease type II - Wikipedia Glycogen storage disease type II (GSD-II), also called Pompe disease, and formerly known as GSD-IIa or Limb–girdle muscular dystrophy 2V, is an autosomal recessive metabolic disorder [1] which damages muscle and nerve cells throughout the body It is caused by an accumulation of glycogen in the lysosome due to a deficiency of the lysosomal acid alpha-glucosidase enzyme (GAA) The inability
Pompe’s disease | Glycogen Storage, Enzyme Deficiency, Muscle . . . While every effort has been made to follow citation style rules, there may be some discrepancies Please refer to the appropriate style manual or other sources if you have any questions Britannica Editors "Pompe’s disease" Encyclopedia Britannica, 19 Feb 2019, https: www britannica com science Pompes-disease Accessed 13 November 2025
Pompe Disease - UF Health Alternative Names GSD II; Glycogen Storage Disease Type II; Cardiomegalia Glycogenica Diffusa; Generalized Glycogenosis, Cardiac Form; Acid Maltase Deficiency; Acid Alpha-Glucosidase Deficiency; GAA Deficiency; Pompe Disease; Glycogenosis Type II; Alpha-1,4-Glucosidase Deficiency; Pompe's Disease; Pompes Disease What is Pompe Disease?
Home - AMDA Pompe The Acid Maltase Deficiency Association formed to assist in funding research and to promote public awareness of Acid Maltase Deficiency, also known as Pompe’s Disease
How Does Pompe’s Disease Affect the Respiratory System? How Is Respiratory Insufficiency Managed in Patients With Pompes Disease? Respiratory difficulties brought on by a weakened diaphragm and chest muscles in Pompe’s disease can be managed by various treatment options
Pompe Disease | PM R KnowledgeNow Pompe Disease (PD), also referred to as Type 2 Glycogenesis or Acid Maltase Deficiency, is a glycogen storage disease that occurs due to an inherited