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Prenatal tests for Sanfilippo disease type B in four pregnancies
Authors:Jean Mossman  Elisabeth P. Young  A. D. Patrick  A. H. Fensom  Marie Ellis  P. P. Benson  V. M. Der Kaloustian
Affiliation:1. Institute of Child Health, London WC1N 1EH, U.K.;2. Paediatric Research Unit, The Prince Philip Research Laboratories, Guy's Hospital Medical School, London SE1 9RT, U.K.;3. Department of Pediatrics, American University of Beirut Hospital, Lebanon
Abstract:We report the prenatal diagnosis of two fetuses with Sanfilippo disease type B. In both pregnancies there were excessive amounts of heparan sulphate in amniotic fluid and the activity of N-acetyl-α-D-glucosaminidase was undetectable in cultured amniotic fluid cells. The predictions were confirmed by enzyme assay of cultured skin fibroblasts from the aborted fetus or the affected infant. The disorder was excluded for two other pregnancies at risk and the predictions are considered to be correct because of the normal progress of the healthy children.
Keywords:Sanfilippo disease type B (MPS IIIB)  N-acetyl-α-D-glucosaminidase  Amniotic fluid  Heparan sulphate
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