mucopolysaccharidosis type 3C

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Natural History to Assess Disease in Patients With MPS IIIC	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mucopolysaccharidosis III, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, connective tissue disorder, cutaneous mucinosis, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, lysosomal storage disease, metabolic disease, mucopolysaccharidosis, mucopolysaccharidosis type 3C	Not yet recruiting	Not stated	2026-07-17		NCT07712003
Natural History Study of Participants With Sanfilippo Syndrome Type IIIC	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mucopolysaccharidosis III, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, connective tissue disorder, cutaneous mucinosis, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, lysosomal storage disease, metabolic disease, mucopolysaccharidosis, mucopolysaccharidosis type 3C	Recruiting	Not stated	2026-05-12		NCT05825131

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