Mucopolysaccharidosis 2 (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 (iduronidate 2-sulfatase) needed to break it down.
See also:
Mucopolysaccharidosis type 2 Hunter syndrome- mild form:
»Introduction: Mucopolysaccharidosis type 2 Hunter syndrome- mild form
»Symptoms of Mucopolysaccharidosis type 2 Hunter syndrome- mild form
These medical condition or symptom topics may be relevant to medical information for Mucopolysaccharidosis 2:
Mucopolysaccharidosis 2: Another name for Mucopolysaccharidosis type 2 Hunter syndrome- mild form (or close medical condition association).
»Introduction: Mucopolysaccharidosis type 2 Hunter syndrome- mild form
»Symptoms of Mucopolysaccharidosis type 2 Hunter syndrome- mild form
Some of the symptoms of Mucopolysaccharidosis 2 incude:
These medical disease topics may be related to Mucopolysaccharidosis 2:
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