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.
Related Articles
Last Modified: 21/06/2007
Related Chat 3
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?
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!
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.
You'll need to be logged in to post new Comments and Answers or to Chat.
Login or
Register