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Advancements in Treating Mucopolysaccharidosis Type I: From Enzyme Replacement to Cutting-Edge Therapies | #hurler syndrome treatment market # hurler scheie syndrome market # laronidase biosimilar # mucopolysaccharidosis type 1 treatment # aldurazyme patent expiration # sanofi mucopolysaccharidosis / mps i # mucopolysaccharidosis type i market # mucopolysaccharidosis treatment # hurler scheie syndrome market forcast # mps type 1 treatment

Advancements in Treating Mucopolysaccharidosis Type I: From Enzyme Replacement to Cutting-Edge Therapies

Advancements in Treating Mucopolysaccharidosis Type I: From Enzyme Replacement to Cutting-Edge Therapies

Mucopolysaccharidosis Type I (MPS I) is a rare lysosomal storage disorder that affects approximately 1 in 100,000 births worldwide. This progressive condition results from mutations in the IDUA gene, which leads to a deficiency of the enzyme alpha-L-iduronidase. Without this crucial enzyme

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