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Advancements in MPS I Treatment: From Enzyme Replacement to Cutting-Edge Therapies

Advancements in MPS I Treatment: From Enzyme Replacement to Cutting-Edge Therapies

Mucopolysaccharidosis Type I is a rare lysosomal storage disorder characterized by the deficiency of alpha-L-iduronidase enzyme, leading to the harmful accumulation of glycosaminoglycans throughout the body.