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Up to: Syndromic disease · Lysosomal storage disease with skeletal involvement · Mucopolysaccharidosis type 1
Hurler-Scheie syndrome
Hurler-Scheie syndrome is the intermediate form of mucopolysaccharidosis type 1 (MPS1) between the two extremes Hurler syndrome and Scheie syndrome ; it is a rare lysosomal storage disease, characterized by skeletal deformities and a delay in motor development.
This condition has no sub-types.