PGT-M Preimplantation Genetic Testing for Monogenic disorders

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

Healthy embryos are selected to be transferred in the IVF process.

Reliable testing in an accredited UK laboratory

PGT-M detects more than 300 genetic diseases.

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.

> Identifies embryos affected with a genetic disorder before transfer

> Custom-designed test for every couple

> In-depth genetic counseling 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.

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