What Is an NT Scan for Down Syndrome? An NT scan, or nuchal translucency scan, is a non-invasive ultrasound screening for Down syndrome and other genetic conditions during pregnancy.

Nuchal fold thickening, short humerus, or a major structural anomaly -- even as an isolated finding -- confers a high enough risk of aneuploidy in both high- and low-risk populations to recommend ...

Although an ultrasound detected an increased nuchal fold thickness in the second trimester, the pregnancy was otherwise uncomplicated.

The presence of multiple sonographic markers during the second trimester is associated with a higher risk for trisomy 21 compared with their absence, but individual markers are less predictive.

Saw the gynae yesterday for the 12 week nuchal fold scan and he said that the growth is either a fibroid or a possible cancerous growth so he ordered the cancer marker bloodtests along with the ...

This test, also called the Nuchal Fold Scan, is a prenatal screening test designed to help your healthcare professional access your baby’s risk for chromosomal abnormalities such as Down ...

Women with singleton pregnancies underwent first-trimester combined screening (measurement of nuchal translucency, pregnancy-associated plasma protein A [PAPP-A], and the free beta subunit of ...

You can have a test for this defect during the second trimester to help you make decisions about your pregnancy. Nuchal fold is the skin at the back of the neck (nape).

What other Down syndrome screening tests are available during pregnancy? Second-trimester ultrasounds aren’t the only screening tests available for Down syndrome.

Optimally, noninvasive screening also includes that a preliminary ultrasound to detect nuchal translucency takes place late in the first trimester.

The standard first-trimester screen for Down syndrome, called the combined test, uses three numbers in an algorithm to assess the chance that the fetus has the genetic disorder: markers from the ...