Introduction: Mucopolysaccharidosis VI


advertisement

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

Misdiagnosis and Mucopolysaccharidosis VI: Research more detailed information about misdiagnosis of Mucopolysaccharidosis VI, or research misdiagnosis of other diseases

Treatments for Mucopolysaccharidosis VI: Various information is available about treatments available for Mucopolysaccharidosis VI, or research treatments for other diseases.

         Contents for Mucopolysaccharidosis VI:

Footnotes:
1. excerpt from NINDS Mucopolysaccharidoses Information Page: NINDS

Medical Tools & Articles:


Next articles:

Medical Articles:
 
 
CureResearch.comTM Copyright © 2010 Health Grades, Inc. All rights reserved.
Home | Contents | Search | Site Map | Feedback | Contact Us | Terms of Use | Privacy Policy | About Us | Advertise