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Mucopolysaccharidosis Type III

Mucopolysaccharidosis Type III: Introduction

Mucopolysaccharidosis Type III: 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 III is available below.

Symptoms of Mucopolysaccharidosis Type III

Treatments for Mucopolysaccharidosis Type III

  • There is no specific treatment for the condition. Treatment is aimed at treating or managing symptoms as they arise
  • more treatments...»

Mucopolysaccharidosis Type III: Deaths

Read more about Deaths and Mucopolysaccharidosis Type III.

Causes of Mucopolysaccharidosis Type III

Read more about causes of Mucopolysaccharidosis Type III.

Mucopolysaccharidosis Type III: Broader Related Topics

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More information about Mucopolysaccharidosis Type III

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

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