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MPS 3 D: Introduction

MPS 3 D: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) due to deficiency of an enzyme called N-acetylglucosamine-6-sulfate sulfatase. Mucopolysaccharide levels build up and are then deposited in various tissues. More detailed information about the symptoms, causes, and treatments of MPS 3 D is available below.

Symptoms of MPS 3 D

Wrongly Diagnosed with MPS 3 D?

MPS 3 D: Deaths

Read more about Deaths and MPS 3 D.

Causes of MPS 3 D

Read more about causes of MPS 3 D.

Disease Topics Related To MPS 3 D

Research the causes of these diseases that are similar to, or related to, MPS 3 D:

MPS 3 D: Broader Related Topics

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Videos about MPS 3 D


More information about MPS 3 D

  1. MPS 3 D: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Deaths

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