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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

PGT-M Preimplantation Genetic Testing

(単一遺伝子疾患の着床前遺伝検査)

PGT-M検査は、遺伝性疾患を遺伝させるリスクのあるカップルをサポートします。この遺伝子検査は、将来生まれてくる赤ちゃんへの遺伝性疾患の遺伝を防ぎ、健康な妊娠を目指します。

詳しくはこちら

ERA®
子宮内膜着床能

良質な胚を損なうことなく、妊娠の確率を最大限高めます。

ERA® 検査は、女性一人ひとりに合わせた胚移植のタイミングを見極め、胚移植と着床のタイミングを連動させる初めての診断検査です。繰り返し着床に失敗した経験のある患者様に適しています。

詳しくはこちら

CGT検査

CGT Carrier Genetic Test

遺伝子疾患は治りませんが、予防することはできます。

CGT検査 は、遺伝子疾患を持つ子供が生まれるリスクを判定することができるため、妊娠を計画する際に極めて有用な遺伝子検査です。

詳しくはこちら

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To see the accreditation certificate, associated technical annex and list of accredited tests, click on this link.

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  • Patient Journey（患者様向け）
    • 妊娠前
    • 体外受精をはじめたら
    • 妊娠中
    • 出産後
  • Reproductive Health
    • Specialists
      • ALICE
      • EMMA
      • ERA
      • EndomeTRIO
      • Infertility Panels
      • EMBRACE
      • PGT-A
      • PGT-A Plus
      • PGT-M
      • PGT-SR
      • CGT
      • NACE
      • Zenit
      • POC Portfolio
      • SAT
      • Newborn Screening
  • Diagnostics
  • About us
    • Igenomix Research
    • About Igenomix
    • Igenomix Worldwide
  • Academy
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