For all Obstetrics scans, no special preparation is needed, although it is best to wear loose clothing that can easily be lifted or removed in...
- A nuchal scan or nuchal translucency (NT) scan/procedure is a sonographic prenatal screening...
- Back to Your pregnancy and baby guide.
- A special ultrasound, called a nuchal translucency screening, risks would allow...
- There are a number of tests and scans available to you during your pregnancy. The nuchal...
There are a number of tests and scans available to you during your pregnancy. The nuchal translucency scan is an ultrasound that may detect the risk of a number of chromosomal abnormalities. A nuchal translucency scan is part of the ultrasound scan that most pregnant women have at around 12 weeks of pregnancy. The results of a nuchal translucency scan may tell you if your baby has a high or low risk of a chromosomal abnormality.
Examples of chromosomal abnormalities include trisomy 21 Down Syndrome , trisomy 18 Edwards Syndrome or trisomy 13 Patau syndrome. The results will tell you if your baby is at high risk or low risk of chromosomal abnormality in comparison to the general population. The nuchal translucency scan is done between 11 and 14 weeks of pregnancy.
Usually the scan is done through your abdomen but occasionally the nuchal translucency can only be seen by inserting a probe into the vagina. You might also be offered a blood test around this time. Your doctor can look at the results of the combined test blood test and nuchal translucency scan to get a more accurate picture of the risk of a chromosomal abnormality.
The results of the nuchal translucency scan will not be used alone to calculate the risk of a chromosomal abnormality.
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