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Our Services > NACE

NACE Non-invasive Prenatal Test

Detects abnormalities, such as Down’s Syndrome with a simple maternal blood test.

  • Overview
  • Features
  • How does it Work?
  • I’m a health specialist

Completely safe for both you and your baby

Test available from week 10

Highest informativity rate: we obtain results for 99.9% of analyzed samples

Overview
  • It is a test that is performed on any pregnant woman to determine the number of chromosomes in the baby, without compromising the foetus or the mother.

Chromosomal normality involves having 23 pairs of chromosomes:

Extra or missing chromosomes can lead to health and developmental problems:

What is NACE test?

  • NACE is a non-invasive prenatal test. This means that it is completely safe for you and your baby: a small blood sample, just like in any other routine blood analysis, is sufficient to perform the test.
  • NACE uses the latest sequencing technology to analyse foetal DNA to detect the most common anomalies with high precision and reliability.

What does NACE detect?

  • NACE® detects abnormalities in chromosomes 21, 18, 13 and the most common anomalies in the sex chromosomes (X and Y).
  • NACE 24 analyses the full set of chromosomes at the resolution of a standard karyotype. It identifies deletions and duplications that are associated with clinically relevant genetic syndromes.

T21: Down Syndrome; T18: Edwards Syndrome; T13: Patau Syndrome; 45, X: Turner Syndrome

 

The turnaround time for NACE and NACE 24 is 10 working days.

Features
  • Benefits
  • Indications

Why use NACE?

  • Non-invasive and risk-free: Analyses the most frequent chromosomal alterations with a simple blood test.
  • Completely safe for you and your baby
  • Helps to avoid unnecessary amniocentesis
  • Option to report fetal sex from week 10
  • Pre- and post-test personalised genetic counselling is available

Who should use NACE?

NACE is available to all pregnant women from week 10 of pregnancy.

This test is recommended if:

  • You want to be more informed about your pregnancy
  • You are at high risk of chromosomal alterations after your first trimester screening
  • You have a previous history of births with chromosomal abnormalities
How does it work?

BROCHURE

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