Clinical review demonstrates variable detection of non-chromosomal abnormalities in first-trimester fetuses, highlighting the influence of gestational timing and scan objectives.
At 11-13 weeks some abnormalities are always detectable, some can never be and others are potentially detectable depending on their association with increased NT, the phenotypic expression of the abnormality with gestation and the objectives set for such a scan.
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Syngelaki et al. (2011) studied this question.
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