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A nuchal translucency (NT) test is an optional ultrasound performed in the first trimester of pregnancy. It helps determine a fetus's risk of congenital conditions like Down syndrome. It’s highly accurate at detecting conditions when combined with other first-trimester screenings. Contents Overview Test Details Results and Follow-Up. Overview.
A nuchal translucency screening, or NT screening, is a specialized routine ultrasound performed at the end of the first trimester of pregnancy. It helps doctors determine if a baby is statistically more likely to have a chromosomal abnormality.
The first trimester screening test (FTS) is blood work, and the nuchal translucency test is specialized imaging of the fetus using ultrasound. When the two tests are performed together, the combined data can help assess the risk of certain genetic conditions, but it cannot diagnose them.
During a test for nuchal translucency (NT), an ultrasound is performed to measure the collection of fluid between the fetus’s spine and the skin in the area of the nape of the neck. The procedure is performed by a specially trained ultrasound technician, and the results are read by a radiologist who also has specific training.
A nuchal scan or nuchal translucency (NT) scan/procedure is a sonographic prenatal screening scan to detect chromosomal abnormalities in a fetus, though altered extracellular matrix composition and limited lymphatic drainage can also be detected.
An NT scan, or nuchal translucency scan, is a non-invasive ultrasound screening for Down syndrome and other genetic conditions during pregnancy. It’s usually done between weeks 11 and 14 of...
The nuchal translucency test (also called the NT scan) uses ultrasound to assess your developing baby's risk of having Down syndrome (DS) and some other chromosomal abnormalities, as well as major congenital heart problems.
What is Nuchal Translucency (NT)? NT is the name given to the black area seen by ultrasound at the back of the fetal head/neck between 11 - 14 weeks of gestation. The NT represents a normal accumulation of fluid, but, if too thick (usually above 3-3,5mm), it is a sign that something may not be going well with the development of your baby.
The nuchal translucency test measures the nuchal fold thickness. This is an area of tissue at the back of an unborn baby's neck. Measuring this thickness helps assess the risk for Down syndrome and other genetic problems in the baby.
The nuchal translucency test measures the nuchal fold thickness. This is an area of tissue at the back of an unborn baby's neck. Measuring this thickness helps assess the risk for Down syndrome and other genetic problems in the baby.