As with every pregnancy, the great excitement is often accompanied by concerns about the baby's health.

One of the recommended tests early in pregnancy is the Nuchal Translucency (NT) Screening.

I’d like to share important information about this test and provide you with all the tools to make an informed decision.

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What is the Nuchal Translucency (NT) Screening?
The NT screening is an ultrasound examination performed between week 11 and week 13+6 of pregnancy.

During the scan, the thickness of the fluid layer at the back of the baby's neck is measured.

This measurement, combined with additional factors such as your age and medical history, allows for a statistical assessment of the risk for Down syndrome and other chromosomal conditions.
 

Why is this test important?

•  Early detection: This test enables the early identification of an increased risk for Down syndrome and other conditions, even before clear findings can be seen in an ultrasound.

• Mental preparation: If the screening indicates an increased risk, follow-up tests can be performed to confirm or rule out the diagnosis, allowing you to prepare accordingly.

• Peace of mind: For most women, the results are reassuring and provide peace of mind.
   

What happens during the test?

• Non-invasive and painless – The scan takes about 10-15 minutes and is performed using an ultrasound device.

• During the test, you will lie on an examination bed, and I will gently move the ultrasound probe over your abdomen.

 

The Nuchal Translucency screening is an important tool for assessing the risk of Down syndrome and other chromosomal abnormalities.

It is important to remember that this test is statistical and does not provide a definitive diagnosis.

If you have any further questions, please don’t hesitate to ask – I’m here for you.