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Hurler-Scheie syndrome

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

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.

Synonyms

  • Hurler-Scheie syndrome
  • Hurler–Scheie syndrome
  • MPS I H-S
  • MPS1-HS
  • MPS1H/S
  • MPSIH/S
  • Scheie disease mps type 1s
  • Scheie's syndrome
  • l-iduronidase deficiency, Scheie type
  • mucopolysaccharidosis IH/S
  • mucopolysaccharidosis type 1H/S
  • mucopolysaccharidosis type I mild form
  • mucopolysaccharidosis type I-S
  • mucopolysaccharidosis type IH/S
  • mucopolysaccharidosis type Ih/S
  • mucopolysaccharidosis, mps-I-sHurler-Scheie syndrome
  • Hurler–Scheie syndrome
  • MPS I H-S
  • MPS1-HS
  • MPS1H/S
  • MPSIH/S
  • Scheie disease mps type 1s
  • Scheie's syndrome
  • l-iduronidase deficiency, Scheie type
  • mucopolysaccharidosis IH/S
  • mucopolysaccharidosis type 1H/S
  • mucopolysaccharidosis type I mild form
  • mucopolysaccharidosis type I-S
  • mucopolysaccharidosis type IH/S
  • mucopolysaccharidosis type Ih/S
  • mucopolysaccharidosis, mps-I-s
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