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MPS VI (medical condition): A lysosomal storage disorder that is caused by a...more »
See also:
Mucopolysaccharidosis VI:
»Introduction: Mucopolysaccharidosis VI
»Symptoms of Mucopolysaccharidosis VI
»Treatments for Mucopolysaccharidosis VI
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:
See full list of 8 symptoms of MPS VI (Mucopolysaccharidosis VI)
Treatments for MPS VI (Mucopolysaccharidosis VI) include:
Read more about treatments for MPS VI
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
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