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Morquio syndrome: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of the enzyme (galactosamine-?-sulfate - type A, ? galactosidase - type B) needed to break it down. The symptoms are variable with type A and B being clinically indistinguishable. More detailed information about the symptoms, causes, and treatments of Morquio syndrome is available below.
See full list of 30 symptoms of Morquio syndrome
Read more about causes of Morquio syndrome.
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Types of Morquio syndrome
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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 Morquio syndrome, or a subtype of Morquio syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Morquio syndrome as a "rare disease".
Source - Orphanet
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