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Results 1 - 10 of 21 for Hurler
  1. Mucopolysaccharidosis type I (MPS I) is a rare disease in which the body is missing or does not have enough of an enzyme needed to ...
  2. ... disorder was once divided into three separate syndromes: Hurler syndrome (MPS I-H), Hurler-Scheie syndrome (MPS I-H/S), and Scheie ... not show signs and symptoms of the condition. Hurler syndrome Hurler-Scheie syndrome IDUA deficiency MPS I ...
  3. Hurler Syndrome (National Marrow Donor Program)  
    ​​​Learn about Hurler syndrome, a genetic condition affecting metabolism. Discover symptoms, treatment options, and how bone marrow transplant (BMT) can help ...
  4. ... III, variant Mucolipidosis IIIC Mucolipidosis type III Pseudo-Hurler polydystrophy Genetic Testing Registry: GNPTG-mucolipidosis National Organization ...
  5. ... Mucolipidosis III Mucolipidosis III, variant Mucolipidosis IIIA Pseudo-Hurler polydystrophy Genetic Testing Registry: Pseudo-Hurler polydystrophy National ...
  6. Mucopolysaccharidoses From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Carbohydrate Metabolism Disorders/Specifics ... Carbohydrate Metabolism Disorders ... National Institute of Neurological Disorders and Stroke ... From the National Institutes ...
  7. ... several other types of MPSs, including: MPS I (Hurler syndrome; Hurler-Scheie syndrome; Scheie syndrome) MPS III (Sanfilippo syndrome) ...
  8. ... several other types of MPSs, including: MPS I (Hurler syndrome; Hurler-Scheie syndrome; Scheie syndrome) MPS II (Hunter syndrome) ...
  9. ... several other types of MPSs, including: MPS I (Hurler syndrome; Hurler-Scheie syndrome; Scheie syndrome) MPS II (Hunter syndrome) ...
  10. ... are several types of MPSs, including: MPS I (Hurler syndrome; Hurler-Scheie syndrome; Scheie syndrome) MPS II (Hunter syndrome) ...
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