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 IH mucopolysaccharidosis (medicine)


type IH mucopolysaccharidosis -->
Hurler's syndrome
<syndrome> Mucopolysaccharidosis in which there is a deficiency of alpha-l-iduronidase, an accumulation of an abnormal intracellular material, and excretion of dermatan sulfate and heparan sulfate in the urine; with severe abnormality in development of skeletal cartilage and bone, with dwarfism, kyphosis, deformed limbs, limitation of joint motion, spadelike hand, corneal clouding, hepatosplenomegaly, mental retardation, and gargoyle-like facies; autosomal recessive inheritance.

See: mucolipidosis.

Synonym: dysostosis multiplex, Hurler's disease, lipochondrodystrophy, Pfaundler-Hurler syndrome, type IH mucopolysaccharidosis.