中国医学前沿杂志（电子版）2017，Vol.9Issue(12)：102-104,3.DOI:10.12037/YXQY.2017.12-23
NT和NF在胎儿染色体异常检测中的应用价值
The application value of NT and NF in the detection of fetal chromosomal abnormalities
安晓玲 1郝荣 1张春燕1
作者信息
- 1. 西北妇女儿童医院 超声科,西安 710061
- 折叠
摘要
Abstract
Objective To analyze the value of nuchal translucency (NT) and nuchal fold (NF) in the detection of fetal chromosomal abnormalities. Method From January 2015 to December 2016, 69 pregnant women who underwent obstetric ultrasonography for NT and NF in our hospital were selected as research subjects. All pregnant women underwent interventional prenatal diagnosis, the detection rates of NT and NF on chromosomal abnormalities were analyzed. Result Ultrasonography showed that there were 35 pregnant women with NT thickening, 8 cases of chromosomal abnormalities found in villus culture, the detection rate was 22.9%. Ultrasonography showed that there were 34 pregnant women with NF thickening, 4 cases of chromosomal abnormalities were found in amniotic fluid culture, the detection rate was 11.8%. Conclusion The thickening of NT and NF in fetal screening of chromosomal abnormalities has an important value in application. Early detection of fetal chromosomal abnormalities in early/middle gestational stages.关键词
染色体异常/颈项透明层/颈后皮肤皱褶Key words
Chromosomal abnormality/Nuchal translucency/Nuchal fold引用本文复制引用
安晓玲,郝荣,张春燕..NT和NF在胎儿染色体异常检测中的应用价值[J].中国医学前沿杂志（电子版）,2017,9(12):102-104,3.
