Genetic examination for fetuses with increased nuchal translucency by exome sequencing.

The journal of obstetrics and gynaecology research(2023)

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摘要
The diagnostic yield of prenatal ES is low for fetuses with an isolated increased NT. In addition to Noonan syndrome, there are additional genetic syndromes such as Kabuki syndrome and Thanatophoric dysplasia type I that are potentially associated with an increased NT. A cut-off of greater than the 95th percentile may be useful in case selection for ES. Whether it is clinically meaningful to monitor NF values for fetuses with isolated increased NT and normal chromosomes worth considering.
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关键词
exome sequencing,genetic counseling,genomic variants,nuchal translucency,prenatal diagnosis
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