Modality: MRI (T2)

- “ Mucopolysaccharidosis type I is an inherited metabolic disorder secondary to enzyme deficiency and an inability to break down glycosaminoglycans. ...”

Used in the following article:

  • Hurler syndrome - “ Hurler syndrome is one of the mucopolysaccharidoses (MPS type I). Epidemiology The estimated incidence is ~1:100,000. Clinical presentation It...”

View full size version of Cerebral manifestations of mucopolysaccharidosis type I

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