首页> 外文期刊>Prenatal Diagnosis >Non-invasive risk assessment of fetal sex chromosome aneuploidy through directed analysis and incorporation of fetal fraction
【24h】

Non-invasive risk assessment of fetal sex chromosome aneuploidy through directed analysis and incorporation of fetal fraction

机译:通过定向分析和整合胎儿分数,对胎儿性染色体非整倍性进行非侵入性风险评估

获取原文
获取原文并翻译 | 示例
           

摘要

Objective: To assess the performance of a directed chromosomal analysis approach in the prenatal evaluation of fetal sex chromosome aneuploidy. Methods: We analyzed 432 frozen maternal plasma samples obtained from patients prior to undergoing fetal diagnostic testing. The cohort included women greater than 18years of age with a singleton pregnancy of greater than 10weeks gestation. Samples were analyzed using a chromosome-selective approach (DANSRTM) and a risk algorithm that incorporates fetal fraction (FORTETM). Results: The cohort included 34 cases of sex chromosome aneuploidy. The assay correctly identified 26 of 27 (92.6%) cases of Monosomy X, one case of XXX, and all six cases of XXY. There were four false positive cases of sex chromosome aneuploidy among 380 euploid cases for an overall false positive rate of less than 1%. Discussion: Analysis of the risk for sex chromosome aneuploidies can be accomplished with a targeted assay with high sensitivity.
机译:目的:评估定向染色体分析方法在胎儿性别染色体非整倍性产前评估中的性能。方法:在接受胎儿诊断测试之前,我们分析了432例冷冻的孕妇血浆样品。该队列包括年龄大于18岁,单胎妊娠大于10周的女性。使用染色体选择性方法(DANSRTM)和包含胎儿分数的风险算法(FORTETM)对样品进行了分析。结果:该队列包括34例性染色体非整倍性。该测定法正确地识别了27例X染色体Monosomy病例中的26例(92.6%),XXX例1例和XXY的全部6例。在380个整倍性病例中,有4个性染色体非整倍性假阳性病例,总假阳性率低于1%。讨论:性染色体非整倍性的风险分析可以通过高灵敏度的靶向分析来完成。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号