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Multiple sulfatase deficiency with early severe retinal degeneration.
Harbord, M; Buncic, J R; Chuang, S A; Skomorowski, M A; Clarke, J T.
Afiliação
  • Harbord M; Department of Pediatrics, Hospital for Sick Children, Toronto, Ontario, Canada.
J Child Neurol ; 6(3): 229-35, 1991 Jul.
Article em En | MEDLINE | ID: mdl-1875023
We report an unusual case of multiple sulfatase deficiency in which neurodegeneration was accompanied by early, severe visual impairment associated with prominent pigmentary retinopathy, suggesting a diagnosis of neuronal ceroid-lipofuscinosis. The levels of arylsulfatases A, B, and C, heparan N-sulfatase, N-acetylgalactosamine-6-sulfate sulfatase, and iduronate-2-sulfate sulfatase were all markedly decreased in cultured skin fibroblasts. Screening tests for mucopolysacchariduria were consistently negative; however, thin-layer chromatographic analysis of isolated urinary glycosaminoglycans showed increased amounts of heparan sulfate.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Limite: Child / Humans / Male Idioma: En Ano de publicação: 1991 Tipo de documento: Article
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Limite: Child / Humans / Male Idioma: En Ano de publicação: 1991 Tipo de documento: Article