Home > Nuchal Translucency Screening Test
The nuchal (say "NEW-kuhl") translucency screening is a test done during pregnancy. It uses ultrasound to measure the thickness of the fluid buildup at the back of the developing baby's neck. If this area is thicker than normal, it can be an early sign of Down syndrome, trisomy 18, or heart problems.
The test is done between 11 and 14 weeks of pregnancy. It may be done as part of the first trimester screening test or the integrated screening test.
This test shows the chance that a baby may have a certain problem. It can't show for sure that a baby has a problem. You would need a diagnostic test, such as chorionic villus sampling (CVS) or amniocentesis, to find out for sure if the baby actually has a problem.
A nuchal translucency test is done to find out the chance that your developing baby (fetus) may be at risk for having Down syndrome or other problems.
You may need a full bladder for the nuchal translucency test. If so, you'll be asked to drink water or other liquids just before the test and to avoid urinating before the test.
Talk with your doctor about any concerns you have regarding the need for the test, its risks, how it will be done, or what the results will mean. To help you understand the importance of this test, fill out the medical test information form(What is a PDF document?).
Most often, a nuchal translucency test is done by a specially trained ultrasound technologist. But it may be done by a radiologist or an obstetrician who has received special training to do this test.
Often you don't need to remove your clothes for the test. You can lift your shirt and push down the waistband of your skirt or pants. If you're wearing a dress, you'll be given a cloth or paper covering to put over your legs during the test.
If you need a full bladder for the test, tell your doctor or ultrasound technologist if your bladder is so full that you're in pain.
During the test:
When the test is done, the gel is wiped off your skin. You can urinate as soon as the test is done.
The test usually takes about 15 to 20 minutes.
During a nuchal translucency test, you may have a feeling of pressure in your bladder. The gel may feel cool when it is first put on your belly. You'll feel a light pressure from the transducer as it passes over your belly.
There are no known risks linked with a nuchal translucency test, either to you or the baby. But you may feel anxious if the test shows there is an increased chance that your baby may have a problem.
Ultrasound is a safe way to check for problems and get information about your developing baby. It doesn't use X-rays or other types of radiation that may harm the baby.
Your doctor will look at the results of the nuchal translucency test to see if the area at the back of the baby's neck is thicker than normal.
2.5 millimeters (mm) or less
More than 2.5 mm
You may not receive information about the test right away. Full results are usually available in 1 or 2 days.
The nuchal translucency test can find out if your developing baby (fetus) is at higher-than-normal risk for problems. But it can't tell for sure that the baby has a problem. You would need another test, called a diagnostic test, to make sure.
The accuracy of this test is based on how often the test correctly finds a problem. For example:
It's possible that a screening test will show that the baby has an increased chance of having a problem when he or she doesn't have the problem. This is called a false-positive test result. And it's also possible that a screening may show that the baby doesn't have a problem when he or she does. This is called a false-negative test result.
Nuchal translucency test results may be affected by:
Talk with your doctor about any concerns you have.
Fischbach F, Dunning MB III (2015). A Manual of Laboratory and Diagnostic Tests, 9th ed. Philadelphia: Wolters Kluwer Health.
American College of Obstetricians and Gynecologists (2016). Screening for fetal aneuploidy. ACOG Practice Bulletin No. 163. Obstetrics and Gynecology, 127(5): e123-e137. DOI: 10.1097/AOG.0000000000001406. Accessed April 6, 2017.
Other Works Consulted
Bianchi DW (2010). Prenatal genetic diagnosis. In CA Gleason, SU Devaskar, eds., Avery's Diseases of the Newborn, 9th ed., pp. 180-185. Philadelphia: Elsevier Saunders.
Pagana KD, Pagana TJ (2010). Mosby's Manual of Diagnostic and Laboratory Tests, 4th ed. St. Louis: Mosby Elsevier.
ByHealthwise StaffPrimary Medical ReviewerSarah Marshall, MD - Family MedicineAdam Husney, MD - Family MedicineKathleen Romito, MD - Family MedicineSpecialist Medical ReviewerSiobhan M. Dolan, MD, MPH - Reproductive Genetics
Current as ofJune 6, 2017
Current as of:
June 6, 2017
Sarah Marshall, MD - Family Medicine & Adam Husney, MD - Family Medicine & Kathleen Romito, MD - Family Medicine & Siobhan M. Dolan, MD, MPH - Reproductive Genetics
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