Mucopolysaccharidosis I: Mucopolysaccharidosis I(MPS I), which includes Hurler, Scheie, and Hurler/Scheie syndromes. Hurler syndrome-the ... more about Mucopolysaccharidosis I.
Mucopolysaccharidosis I: Disorder of mucopolysaccharide metabolism in infants. More detailed information about the symptoms, causes, and treatments of Mucopolysaccharidosis I is available below.
Read more about complications of Mucopolysaccharidosis I.
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Medical research articles related to Mucopolysaccharidosis I include:
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Prognosis for Mucopolysaccharidosis I: Poor. Usually death by age 10.
More about prognosis of Mucopolysaccharidosis I
Visit our research pages for current research about Mucopolysaccharidosis I treatments.
The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Mucopolysaccharidosis I include:
See full list of 12 Clinical Trials for Mucopolysaccharidosis I
Types of Mucopolysaccharidosis I
Read more about Types of Mucopolysaccharidosis I
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Mucopolysaccharidosis I(MPS I), which includes Hurler, Scheie, and Hurler/Scheie syndromes. Hurler syndrome-the most severe form of the mucopolysaccharidoses -occurs in infancy with symptoms such as clouding of the cornea and progressive physical and mental disability. Death usually occurs before age 10. Patients with Scheie syndrome experience milder symptoms and have normal intelligence, while those with Hurler/Scheie syndrome suffer from intermediate symptoms. (Source: excerpt from NINDS Mucopolysaccharidoses Information Page: NINDS)
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