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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?
          • 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?

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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 test

          NACE

          Non-invasive prenatal screening helps to avoid unnecessary amniocentesis

          More information

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