广州医药 ›› 2024, Vol. 55 ›› Issue (10): 1122-1128.DOI: 10.20223/j.cnki.1000-8535.2024.10.004

• 论著 • 上一篇    下一篇

NIPT筛查胎儿患猫叫综合征的初探

肖雪1, 赖晓岚1, 刘海量2, 王宇琦1, 赵翠柳1   

  1. 1 暨南大学附属广州红十字会医院妇产科(广东广州 510220);
    2 东莞博奥木华科技有限公司(广东东莞 523808)
  • 收稿日期:2024-03-20 出版日期:2024-10-20 发布日期:2024-11-05
  • 通讯作者: 赵翠柳,E-mail:cao_cheng@hotmail.com
  • 基金资助:
    国家重点研发计划(2016YFC1000703); 广州市卫生和计划生育科技项目(20231A010018)

Application of non-invasive prenatal testing for the screening of fetal Cri du Chat Syndrome

XIAO Xue1, LAI Xiaolan1, LIU Hailiang2, WANG Yuqi1, ZHAO Cuiliu1   

  1. 1 Department of Obstetrics and Gynecology,Guangzhou Red Cross Hospital,Jinan University,Guangzhou 510220,China;
    2 Dongguan Bo'ao Muhua Technology Co.,Ltd.,Dongguan 523808,China
  • Received:2024-03-20 Online:2024-10-20 Published:2024-11-05

摘要: 目的 初步探讨无创产前基因检测(NIPT)筛查胎儿患猫叫综合征临床性能。方法 收集2018年4月—2019年3月行NIPT提示胎儿患猫叫综合征高风险的孕妇,并收集其羊水细胞培养染色体核型分析或微阵列芯片检测结果,分析NIPT与羊水产前诊断结果的符合率。结果 NIPT提示猫叫综合征病例11例,孕妇均接受了羊水穿刺,染色体核型分析或微阵列芯片检测出胎儿染色体异常6例,符合率为54.5%。结论 NIPT对胎儿猫叫综合征的筛查具有临床价值,当提示高风险时必须行有创性产前诊断。

关键词: 无创产前检测, 猫叫综合征, 微缺失/微重复, 产前诊断

Abstract: Objective To investigate the value of non-invasive prenatal testing(NIPT)for the screening of fetal Cri du Chat Syndrome(CdCS). Methods Pregnant women who accepted NIPT with the results with high risk of fetal CdCS were selected in the study from April 2018 to March 2019.They were also accepted prenatal genetic counseling and the chromosome karyotype analysis or CMA detection of amniotic fluid cell culture.The coincidence rate of NIPT with chromosome karyotype and microarray analysis results were conducted. Results There were 11 cases with high risk of fetal CdCS in NIPT.All of them had received amniocentesis chromosome karyotype or microarray analysis,6(54.5%)cases were confirmed. Conclusions NIPT has some clinical value in screening fetal CdCS from maternal blood.Therefore,it was suggested to perform the invasive chromosomal karyotyping and CMA for high risk of fetal CdCS.

Key words: NIPT, Cri du Chat Syndrome, microdeletion/microduplication, prenatal diagnosis