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Our Services > PGT-M

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?
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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

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.

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?

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Other services

CGT Carrier Genetic Test

CGT

Determines the risk of having a child with a genetic disease

More information

PGT-A Preimplantation Genetic Testing

PGT-A

Improves the chances of reproductive success by selecting chromosomally normal embryos

More information

NACE

Non-invasive prenatal screening helps to avoid unnecessary amniocentesis

More information

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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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We guide you
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
- Igenomix Research
- About Igenomix
Webinars
Blog
International
+34 96 390 53 10
Clinic Portal
Request Information