glycogen storage disease due to GLUT2 deficiency

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Accuracy of Home Lactate Meter and Accu-chek Glucometer in Patients With Glycogen Storage Disease	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Fanconi renotubular syndrome, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Nutritional and Metabolic Diseases, Urogenital Diseases, disorder of glycogen metabolism, glycogen storage disease I, glycogen storage disease Ib, glycogen storage disease due to GLUT2 deficiency, glycogen storage disease due to glucose-6-phosphatase deficiency type IA, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, kidney disorder, metabolic disease, renal tubular transport disease, urinary system disorder	Recruiting	Not stated	2026-06-01		NCT07459582

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