Answers are grounded in this paper and cite their sources.
A routine 11-13-week scan, carried out according to a standardized protocol, can identify many severe non-chromosomal fetal abnormalities. A summary statistic of the performance of the first-trimester scan is futile because some abnormalities are always detectable, whereas others are either non-detectable or sometimes detectable. To maximize prenatal detection of abnormalities, additional scans in both the second and third trimesters are necessary.
No takes yet. Share an insight, caveat, or question.
Syngelaki et al. (2019) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: