See what questions
a doctor would ask.
MPS VI (medical condition): A lysosomal storage disorder that is caused by a deficiency of the ability to...more »
These medical condition or symptom topics may be relevant to medical information for MPS VI:
MPS VI is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that MPS VI, or a subtype of MPS VI,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
MPS VI: Another name for Mucopolysaccharidosis VI (or close medical condition association).
»Introduction: Mucopolysaccharidosis VI
»Symptoms of Mucopolysaccharidosis VI
»Treatments for Mucopolysaccharidosis VI
MPS VI: MPS VI is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of MPS VI incude:
Treatments for MPS VI (Mucopolysaccharidosis VI) include:
Treatment of MPS VI: For more treatment information about MPS VI, see treatment of Mucopolysaccharidosis VI (MPS VI)
MPS VI, or Maroteauz-Lamy syndrome, resembles Hurler syndrome. Onset is in infancy, however, ... (Source: excerpt from NINDS Mucopolysaccharidoses Information Page: NINDS)
These medical disease topics may be related to MPS VI:
Source - NIH
Search to find out more about MPS VI:
Search Specialists by State and City