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Mucopolysaccharidosis type 6

Mucopolysaccharidosis type 6: Introduction

Mucopolysaccharidosis type 6: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of the enzyme (Arylsulfatase ?) needed to break it down. More detailed information about the symptoms, causes, and treatments of Mucopolysaccharidosis type 6 is available below.

Symptoms of Mucopolysaccharidosis type 6

Mucopolysaccharidosis type 6: Deaths

Read more about Deaths and Mucopolysaccharidosis type 6.

Mucopolysaccharidosis type 6: Complications

Read more about complications of Mucopolysaccharidosis type 6.

Causes of Mucopolysaccharidosis type 6

Read more about causes of Mucopolysaccharidosis type 6.

Disease Topics Related To Mucopolysaccharidosis type 6

Research the causes of these diseases that are similar to, or related to, Mucopolysaccharidosis type 6:

Less Common Symptoms of Mucopolysaccharidosis type 6

Evidence Based Medicine Research for Mucopolysaccharidosis type 6

Medical research articles related to Mucopolysaccharidosis type 6 include:

Click here to find more evidence-based articles on the TRIP Database

Research about Mucopolysaccharidosis type 6

Visit our research pages for current research about Mucopolysaccharidosis type 6 treatments.

Statistics for Mucopolysaccharidosis type 6

Mucopolysaccharidosis type 6: Broader Related Topics

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Definitions of Mucopolysaccharidosis type 6:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Mucopolysaccharidosis type 6 as a "rare disease".
Source - Orphanet

Related Mucopolysaccharidosis type 6 Info

Videos about Mucopolysaccharidosis type 6

 

More information about Mucopolysaccharidosis type 6

  1. Mucopolysaccharidosis type 6: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Deaths
  6. Complications
 

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