Nuchal Translucency Test

Nuchal Translucency Test


The nuchal translucency scan is part of your first trimester screen and is performed around 11-14 weeks of pregnancy in combination with a blood test to screen your baby for signs of chromosomal disorders such as Down syndrome.

 

There are several factors that help to assess your risk of having a baby with Down syndrome along with the scan itself. His heart rate will be monitored (babies with a high heart rate are more likely to have Down syndrome); your age will be factored in and a blood sample will be taken.

 

During the scan, fluid beneath the skin at the back of your baby’s neck will be measured – babies with Down syndrome tend to have have a thicker layer of fluid in this part of their bodies. The scan identifies 85 percent of babies with the abnormality, but around 5 percent of normal pregnancies will get a positive test result.

 

It’s important to remember that this is a screening test and can’t diagnose abnormalities. If your risk is high you may be offered a diagnostic test called chorionic villus sampling (CVS), which can be carried out between weeks 10 and 13; or an amniocentisis between weeks 14 and 20.

 

The information in this feature is intended for educational purposes only. If you have any concerns about your health, the health of your child or the health of someone you know, please consult with a doctor or other healthcare professional.

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Last Modified: 21/06/2007
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Related Chat 3

etennant
Reply etennant 1 years ago
thanks lilibeez
Its good to know i have my nuchal scan in3wks im really nervous because of my age,my first scan was really clear,heartbeat was strong,baby was moving lots,so hopefully these are all good signs but its still early days!
We have to pay for the nuchal scan here in Aberdeen, £240.00 was that the same for you?
shellbelle1
Reply shellbelle1 1 years ago
At my first scan it was detected that my baby had a thicker than normal nuchal fold (3.8mm) after going through CVS and amnio testing it was found the chromosomes in my baby did not match that of the placenta. This was very rare but the doctors reassured me that they could not find anything wrong with my baby through ultrasound. After more culturing and blood tests all results at 28 weeks pregnant came back fine.
I hope this is reassuring to anyone else in this situation.
thanks lilibeez
Its good to know i have my nuchal scan in3wks im really nervous because of my age,my first scan was really clear,heartbeat was strong,baby was moving lots,so hopefully these are all good signs but its still early days!
lilibeez
Reply lilibeez 1 years ago
At my first scan it was detected that my baby had a thicker than normal nuchal fold (3.8mm) after going through CVS and amnio testing it was found the chromosomes in my baby did not match that of the placenta. This was very rare but the doctors reassured me that they could not find anything wrong with my baby through ultrasound. After more culturing and blood tests all results at 28 weeks pregnant came back fine.
I hope this is reassuring to anyone else in this situation.
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