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采用绒毛取样法对泰-萨克斯病进行产前诊断。

Prenatal diagnosis for Tay-Sachs disease using chorionic villus sampling.

作者信息

Grebner E E, Jackson L G

出版信息

Prenat Diagn. 1985 Sep-Oct;5(5):313-20. doi: 10.1002/pd.1970050503.

Abstract

Prenatal diagnosis for Tay-Sachs disease was performed on 25 patients using chorionic villus sampling (CVS). Nineteen were diagnosed as normal, and six were affected. Normal villus extracts had both hexosaminidase (hex) A and B activity, as determined by Cellogel and polyacrylamide gel electrophoresis, while extracts from affected fetuses had only hex B activity. Compared to cultured amniotic fluid cells or fibroblasts, villi contained less hex A. Hex A levels in fresh villi and cultured trophoblasts were roughly comparable.

摘要

对25例患者采用绒毛取样(CVS)进行了泰-萨克斯病的产前诊断。19例被诊断为正常,6例患病。通过细胞凝胶电泳和聚丙烯酰胺凝胶电泳测定,正常绒毛提取物同时具有己糖胺酶(hex)A和B活性,而患病胎儿的提取物仅具有hex B活性。与培养的羊水细胞或成纤维细胞相比,绒毛中含有的hex A较少。新鲜绒毛和培养的滋养层细胞中的hex A水平大致相当。

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Prenatal diagnosis of Tay-Sachs disease: studies on the reliability of hexosaminidase levels in amniotic fluid.
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