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Mucopolysaccharidosis type 3

Mucopolysaccharidosis type 3: Introduction

Mucopolysaccharidosis type 3: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans). This occurs due to there being not enough of the enzyme called N-acetyl-alpha-glucosaminidase (B) which is needed to break down the mucopolysacharides. The mucopolysaccharides are then deposited in various tissues. More detailed information about the symptoms, causes, and treatments of Mucopolysaccharidosis type 3 is available below.

Symptoms of Mucopolysaccharidosis type 3

Mucopolysaccharidosis type 3: Deaths

Read more about Deaths and Mucopolysaccharidosis type 3.

Causes of Mucopolysaccharidosis type 3

Read more about causes of Mucopolysaccharidosis type 3.

Disease Topics Related To Mucopolysaccharidosis type 3

Research the causes of these diseases that are similar to, or related to, Mucopolysaccharidosis type 3:

Evidence Based Medicine Research for Mucopolysaccharidosis type 3

Medical research articles related to Mucopolysaccharidosis type 3 include:

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Research about Mucopolysaccharidosis type 3

Visit our research pages for current research about Mucopolysaccharidosis type 3 treatments.

Statistics for Mucopolysaccharidosis type 3

Mucopolysaccharidosis type 3: Broader Related Topics

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Definitions of Mucopolysaccharidosis type 3:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Mucopolysaccharidosis type 3 as a "rare disease".
Source - Orphanet

Related Mucopolysaccharidosis type 3 Info

Videos about Mucopolysaccharidosis type 3

 

More information about Mucopolysaccharidosis type 3

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

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