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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.
See full list of 32 symptoms of Nonkeratan-sulfate-excreting Morquio syndrome
Read more about causes of Nonkeratan-sulfate-excreting Morquio syndrome.
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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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