Dictionary > Type ii mucopolysaccharidosis

Type ii mucopolysaccharidosis

type II mucopolysaccharidosis –>
Hunter’s syndrome
(Science: syndrome) An error of mucopolysaccharide metabolism characterised by deficiency of iduronate sulfatase, with excretion of dermatan sulfate and heparan sulfate in the urine; clinically similar to hurler’s syndrome but distinguished by less severe skeletal changes, no corneal clouding, and x-linked recessive inheritance.
Synonym: type II mucopolysaccharidosis.

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