Fetal nuchal translucency thickness (NT) at the 11-14 week scan has been co
mbined with maternal age to provide an effective method of screening for tr
isomy 21;for an invasive testing rate of 5%, about 75% of trisomic pregnanc
ies can be identified. When maternal serum free-beta-human chorionic gonado
tropin and pregnancy-associated plasma protein-A at 11-14 weeks are also ta
ken into account, the detection rate of chromosomal defects is about 90%. I
ncreased NT can also identify a high proportion of other chromosomal abnorm
alities and is associated with major defects of the heart and great arterie
s, and a wide range of skeletal dysplasias and genetic syndromes. Other ben
efits of the 11-14 week scan include early diagnosis of major fetal defects
and the detection of multiple pregnancies, as well as reliable identificat
ion of chorionicity. As with the introduction of any new technology into ro
utine clinical practice, it is essential that those undertaking the 11-14 w
eek scan are adequately trained and that their results are subjected to rig
orous audit.