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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.

NACE Non-invasive prenatal test
  • Overview
  • Features
  • How does it Work?
  • I’m a health specialist
SAT Sperm aneuploidy test

Enjoy a peaceful and healthy pregnancy

Completely safe for both you and your baby

igenomix

Test available from week 10

Highest informativity rate: we obtain results for 99% of analyzed samples

Overview

What is Non-Invasive Prenatal Test?

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

Chromosomal normality involves having 23 pairs of chromosomes:

Extra or missing chromosomes leads 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 fetal DNA to detect the most common anomalies with high precision and reliability.

2 NACE options according to your needs

  • NACE 24 analyzes 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

NACE Non-invasive prenatal test
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 personalized 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 enjoy a peaceful and healthy 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?
NACE Non-invasive prenatal test

BROCHURE

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Other services

PGT-M Preimplantation Genetic Testing

PGT-M

Prevents the transmission of single gene disorders

More information

ERA

Avoid implantation failure by establishing the best day and time for embryo transfer

More information
CGT Carrier Genetic Test

CGT

Determines the risk of having a child with a genetic disease

More information

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  • We guide you
    • Fertility
      • What to do if…
    • Prevent Inherited Diseases
      • Carrier Genetic Test
    • Worry-free Pregnancy
      • NACE
      • Prenatal Diagnostics
      • Newborn Health
  • Reproductive Health
    • Specialists
      • ALICE
      • EMMA
      • ERA
      • EndomeTRIO
      • EMBRACE
      • CGT
      • NACE
      • PGT-A
      • PGT-M
      • POC
      • SAT
      • Newborn Screening
    • Patients
      • ALICE
      • EMMA
      • ERA
      • EndomeTRIO
      • EMBRACE
      • CGT
      • NACE
      • PGT-A
      • PGT-M
      • SAT
      • POC
  • Diagnostics
  • About us
    • Research & Igenomix Foundation
    • About Igenomix
  • Webinars
  • Blog
  • Europe
  • +34 96 390 53 10 Request Information