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Mucopolysaccharidosis type I Scheie syndrome

Mucopolysaccharidosis type I Scheie syndrome: Introduction

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

Symptoms of Mucopolysaccharidosis type I Scheie syndrome

Wrongly Diagnosed with Mucopolysaccharidosis type I Scheie syndrome?

Mucopolysaccharidosis type I Scheie syndrome: Deaths

Read more about Deaths and Mucopolysaccharidosis type I Scheie syndrome.

Causes of Mucopolysaccharidosis type I Scheie syndrome

Read more about causes of Mucopolysaccharidosis type I Scheie syndrome.

Disease Topics Related To Mucopolysaccharidosis type I Scheie syndrome

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

Less Common Symptoms of Mucopolysaccharidosis type I Scheie syndrome

Mucopolysaccharidosis type I Scheie syndrome: Broader Related Topics

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More information about Mucopolysaccharidosis type I Scheie syndrome

  1. Mucopolysaccharidosis type I Scheie syndrome: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Deaths
 

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