医学
胎儿游离DNA
产前筛查
妇产科学
非整倍体
遗传咨询
产前诊断
基因检测
产前护理
妇科
产科
家庭医学
胎儿
怀孕
内科学
遗传学
人口
基因
染色体
环境卫生
生物
作者
Taylor M. Dunn,Akila Subramaniam
标识
DOI:10.1016/j.ogc.2023.03.005
摘要
The number of prenatal genetic screening options, including aneuploidy screening and carrier screening, has drastically increased with rapid advancements in DNA sequencing technologies. Noninvasive prenatal screening analyzing cell-free DNA has quickly been integrated into routine prenatal care as it is the most sensitive and specific screening method for pregnancies at increased and average risk of fetal aneuploidy. The aim of this article is to outline current recommendations for cell-free DNA screening and carrier screening, important aspects of pretest and posttest counseling for obstetric providers, and which patients should be referred to a genetic specialist.
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