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PGT-M Preimplantation Genetic Testing for Monogenic disorders

Prevent the transmission of inherited disorders to future children and achieve a healthy pregnancy

PGT-M Preimplantation Genetic Testing
  • Overview
  • Features
  • How does it Work?
  • I’m a health specialist
igenomix

PGT-M helps couples with a risk of transmitting a genetic disease

POC Products of Conception

Healthy embryos are selected to be transferred in the IVF process

CGT Carrier Genetic Test

PGT-M detects more than 300 genetic diseases

Overview

What are chromosomes and genes?

  • In a person, each cell contains chromosomes that were inherited from each parent, 23 from the father and 23 from the mother. Therefore, each person has two pairs of 23 chromosomes or 46 total chromosomes.
  • Chromosomes are comprised of molecules called DNA.
  • Our DNA is organized into small fragments called genes.
  • When the function of the gene is altered by a change, called mutation, in the specific sequence, a monogenic disease results.

What is PGT-M test?

  • PGT-M (formerly PGD) helps significantly decrease the chance of having a child with an inherited genetic disorder by analysing embryos before transfer and identifying those that do not carry the altered, disease-causing gene.
Features
  • Benefits
  • Indications

Why use Preimplantation Genetic Testing for Monogenic disorders (PGT-M)?

  • Identifies embryos affected with a genetic disorder prior to transfer
  • Custom-designed test for every couple
  • In-depth genetic counselling sessions available at no extra cost
  • Igenomix understands that each patient and situation is unique. We always aim to adapt our testing to meet your needs.

Is PGT-M for you?

This test is recommended if:

  • You already have a child affected by a monogenic disease.
  • You or your partner are carriers or have been diagnosed with one of these diseases or if there is a family history of them

PGT-M is regulated by the HFEA in the UK. If you are working with a clinic in the UK, your clinical team will be able to give you guidance about these regulations and how they may affect you.

How does it work?

Other services

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

PGT-A

PGT-A Preimplantation Genetic Testing

(着床前胚染色体異数性検査)

PGT-A検査は、体外受精で得た胚の遺伝子検査で、妊娠の成功と健康な赤ちゃんの誕生に役立つものです。PGT-A検査により、健康な妊娠のチャンスを増やすことができます。

詳しくはこちら

NACE検査

NACE Non-invasive prenatal test

非侵襲性の出生前検査

Nace検査は、簡単な血液検査でダウン症などの異常を調べることができます。
胎児や母体を危険にさらすことなく、赤ちゃんの染色体数を調べるため、どの妊婦さんにも実施可能な検査です。

詳しくはこちら

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Fertility
Inherited diseases prevention
Healthy pregnancy

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
  • Blog
  • Country/Region
  • +34 96 390 53 10
  • Clinic Portal
  • Request Information

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