The mucopolysaccharidoses types I, II, and 3: urinary findings in 23 cases.

Gordon, B A; Haust, M D

Gordon, B A; Haust, M D.

Clin Biochem ; 3(3): 203-15, 1970 Sep.

Article in En | MEDLINE | ID: mdl-4258598

Subject(s)

Carbohydrate Metabolism, Inborn Errors/urine; Glycosaminoglycans/metabolism; Glycosaminoglycans/urine; Intellectual Disability/urine; Mucopolysaccharidosis II/genetics; Mucopolysaccharidosis II/urine; Mucopolysaccharidosis I/genetics; Mucopolysaccharidosis I/urine; Retinitis Pigmentosa/urine; Adolescent; Child; Child, Preschool; Chromatography, Gas; Chromatography, Gel; Chromatography, Ion Exchange; Female; Galactosamine/urine; Glucosamine/urine; Glycosaminoglycans/analysis; Hexosamines/urine; Humans; Hyaluronoglucosaminidase; Infant; Male; Sulfates/urine; Testis/enzymology; Uronic Acids/urine

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Collection: 01-internacional Database: MEDLINE Main subject: Carbohydrate Metabolism, Inborn Errors / Retinitis Pigmentosa / Mucopolysaccharidosis II / Mucopolysaccharidosis I / Glycosaminoglycans / Intellectual Disability Type of study: Diagnostic_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Clin Biochem Year: 1970 Type: Article

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