Medical Definition of Type IH mucopolysaccharidosis

1. 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. (05 Mar 2000)

Lexicographical Neighbors of Type IH Mucopolysaccharidosis

type 2 dextrocardia
type 2 diabetes
type 2 glycogenosis
type 3 dextrocardia
type 3 glycogenosis
type 4 dextrocardia
type 4 glycogenosis
type 5 glycogenosis
type 6 glycogenosis
type 7 glycogenosis
type A
type AB
type A behaviour
type B
type B behaviour
type IH mucopolysaccharidosis (current term)
type III acrocephalosyndactyly
type III collagen
type III familial hyperlipoproteinaemia
type III hyperlipoproteinaemia
type III hypersensitivity reaction
type III mucopolysaccharidosis
type II acrocephalosyndactyly
type II cells
type II collagen
type II diabetes
type II dip
type II error
type II errors
type II familial hyperlipoproteinaemia

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