polyglucosan body myopathy type 2

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Rare Glycogen Storage Diseases Natural History Study	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Danon disease, Muscular Disorders, Atrophic, Neurobehavioral Manifestations, Neurologic Manifestations, Nutritional and Metabolic Diseases, X-linked disease, cardiomyopathy, cardiovascular disorder, disorder of glycogen metabolism, glycogen storage disease VII, glycogen storage disease due to aldolase A deficiency, glycogen storage disease due to muscle and heart glycogen synthase deficiency, glycogen storage disease due to muscle beta-enolase deficiency, glycogen storage disease due to phosphoglycerate mutase deficiency, glycogen storage disorder due to hepatic glycogen synthase deficiency, heart disorder, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, intellectual disability, metabolic disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular disease, polyglucosan body myopathy 1 with or without immunodeficiency, polyglucosan body myopathy type 2	Recruiting	Not stated	2026-01-07		NCT06795152

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