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Nonkeratan-sulfate-excreting Morquio syndrome

Nonkeratan-sulfate-excreting Morquio syndrome: Introduction

Nonkeratan-sulfate-excreting Morquio syndrome: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of certain enzymes needed to break it down. This disorder is distinguished form other similar conditions by the fact that no keratosulfate is excreted in the urine. More detailed information about the symptoms, causes, and treatments of Nonkeratan-sulfate-excreting Morquio syndrome is available below.

Symptoms of Nonkeratan-sulfate-excreting Morquio syndrome

Causes of Nonkeratan-sulfate-excreting Morquio syndrome

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Definitions of Nonkeratan-sulfate-excreting Morquio syndrome:

Nonkeratan-sulfate-excreting Morquio syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Nonkeratan-sulfate-excreting Morquio syndrome, or a subtype of Nonkeratan-sulfate-excreting Morquio syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Nonkeratan-sulfate-excreting Morquio syndrome

  1. Nonkeratan-sulfate-excreting Morquio syndrome: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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