Medical Definition of Mucopolysaccharidosis I

1. Systemic lysosomal storage disease caused by a deficiency of alpha-l-iduronidase and characterised by progressive physical deterioration with urinary excretion of dermatan sulfate and heparan sulfate. There are three recognised phenotypes representing a spectrum of clinical severity from severe to mild: hurler's syndrome, hurler-scheie syndrome and scheie's syndrome (formerly mucopolysaccharidosis v). Symptoms may include dwarfism, hepatosplenomegaly, gargoyle-like facies, corneal clouding, cardiac complications, and noisy breathing. (12 Dec 1998)

Lexicographical Neighbors of Mucopolysaccharidosis I

muconic acid
muconolactone delta-isomerase
mucopeptide
mucopeptide glycohydrolase
mucopeptides
mucoperichondrial flap
mucoperiosteal
mucoperiosteal flap
mucoperiosteum
mucopolysaccharidase
mucopolysaccharide
mucopolysaccharide keratin dystrophy
mucopolysaccharides
mucopolysaccharidoses
mucopolysaccharidosis
mucopolysaccharidosis I (current term)
mucopolysaccharidosis II
mucopolysaccharidosis III
mucopolysaccharidosis IV
mucopolysaccharidosis vi
mucopolysaccharidosis vii
mucopolysacchariduria
mucoprotein
mucoproteins
mucopurulent
mucopurulent conjunctivitis
mucopus
mucor
mucorales
mucormycosis

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