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Mucopolysaccharidosis type IVB (subtype) (medical condition): 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.
See also:
Morquio syndrome:
»Introduction: Morquio syndrome
»Symptoms of Morquio syndrome
These medical condition or symptom topics may be relevant to medical information for Mucopolysaccharidosis type IVB (subtype):
Mucopolysaccharidosis type IVB (subtype) is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Mucopolysaccharidosis type IVB (subtype), or a subtype of Mucopolysaccharidosis type IVB (subtype),
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Mucopolysaccharidosis type IVB (subtype): Another name for Morquio syndrome (or close medical condition association).
»Introduction: Morquio syndrome
»Symptoms of Morquio syndrome
Some of the symptoms of Mucopolysaccharidosis type IVB (subtype) incude:
See full list of 30 symptoms of Mucopolysaccharidosis type IVB (subtype) (Morquio syndrome)
These medical disease topics may be related to Mucopolysaccharidosis type IVB (subtype):
Source - NIH
Search to find out more about Mucopolysaccharidosis type IVB (subtype):
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