Skip to content
  • Brazil
  • Canada
  • Europe
  • India
  • Italy
  • Japan
  • Korea
  • Latam
  • Spain
  • Taiwan
  • The Middle East
  • Turkey
  • United Kingdom
  • United States
  • +1 (905) 565-9495 Request Information
  • French
  • Part of brands: |
  • Part of brands: |
  • PATIENT JOURNEY
    • Before Pregnant
    • IVF Process
    • Healthy pregnancy
    • After birth
  • Reproductive Health
    • Specialists
      • ERA
      • EndomeTRIO
      • EMMA
      • ALICE
      • CGT
      • PGT-A Plus
      • PGT-A
      • PGT-SR
      • EMBRACE
      • PGT-M
      • NACE
      • POC Portfolio
      • SAT
      • Infertility Panels
  • Kit Request
  • Genetic Counselling
  • About us
    • Igenomix Research
    • About Igenomix
  • Academy
  • CFAS 2023
  • Webinars
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

Enjoy a peaceful and healthy pregnancy

Completely safe for both you and your baby

Test available from week 10

Highest informativeness rate in the market: we obtain results for 99.9% of the analyzed samples

Overview

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.

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 Extended analyzes all 24 chromosomes and identifies microdeletions associated with 6 major genetic syndromes.

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

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

Features

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
How does it work?

Brochure

Download
email

Subscribe to
our newsletter

Other services you may be interested

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
Determines the risk of having a child with a genetic disease

More information

Igenomix is in the media

Igenomix is not affiliated with any news outlet or publication identified above. News coverage does not constitute an endorsement of Igenomix or its products.

WE GUIDE YOU

Fertility
Inherited diseases prevention
Healthy pregnancy

OUR SERVICES

Genetic solutions
Learn about genetics

ABOUT US

About Igenomix
Contact
Quality
Work with us

FOLLOW IGENOMIX

*CAP accreditation applies to the LA lab.

  +1 (905) 565-9495  fax +1 (905) 671-1938
  Email us
  • Brazil
  • Canada
  • Europe
  • India
  • Italy
  • Japan
  • Korea
  • Latam
  • Spain
  • Taiwan
  • The Middle East
  • Turkey
  • United Kingdom
  • United States
Language

[2024] © Igenomix Privacy policy Quality policy Terms & conditions User Feedback

Request Information

  • PATIENT JOURNEY
    • Before Pregnant
    • IVF Process
    • Healthy pregnancy
    • After birth
  • Reproductive Health
    • Specialists
      • ERA
      • EndomeTRIO
      • EMMA
      • ALICE
      • CGT
      • PGT-A Plus
      • PGT-A
      • PGT-SR
      • EMBRACE
      • PGT-M
      • NACE
      • POC Portfolio
      • SAT
      • Infertility Panels
  • Kit Request
  • Genetic Counselling
  • About us
    • Igenomix Research
    • About Igenomix
  • Academy
  • CFAS 2023
  • Webinars
  • French
  • Canada