See Also: type I H-2fS mucopolysaccharidosis(medicine)
type III mucopolysaccharidosis(medicine)
type IVA,B mucopolysaccharidosis(medicine)
type V mucopolysaccharidosis(medicine)
type VI mucopolysaccharidosis(medicine)
type VII mucopolysaccharidosis(medicine)
type II mucopolysaccharidosis(medicine)
type IH mucopolysaccharidosis(medicine)
type IS mucopolysaccharidosis(medicine)
type VIII mucopolysaccharidosis(medicine)

type III mucopolysaccharidosis (medicine)


type III mucopolysaccharidosis -->
Sanfilippo's syndrome
<syndrome> An error of the mucopolysaccharide metabolism, with excretion of large amounts of heparan sulfate in the urine and severe mental retardation with hepatomegaly; skeleton may be normal or may present mild changes similar to those in Hurler's syndrome; several different types (A, B, C, and D) have been identified according to the enzyme deficiency; autosomal recessive inheritance.

Synonym: type III mucopolysaccharidosis.