Introduction: Mucopolysaccharidosis VI
Mucopolysaccharidosis VI: Disorder of mucopolysaccharide metabolism in infants.
Mucopolysaccharidosis VI: MPS VI, or Maroteauz-Lamy syndrome, resembles Hurler syndrome. Onset is in infancy, however, intelligence is normal. Individuals may live into the second or third decade. 1
Treatments for Mucopolysaccharidosis VI:
Various information is available about treatments available for Mucopolysaccharidosis VI,
or research treatments for other diseases.
|Contents for Mucopolysaccharidosis VI:|
1. excerpt from NINDS Mucopolysaccharidoses Information Page: NINDS
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