PGT-M - Canada

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 analyzing embryos before transfer. The PGT-M:

Analyzes the DNA of each embryo
Identifies healthy embryos
Helps the doctor determine which embryo to transfer

Features

Benefits
Indications

Why use PGT-M?

Identifies embryos affected with a genetic disorder prior to transfer.
Unique probe custom-designed for every patient.
In-depth genetic counseling sessions available at no extra cost.
Igenomix understands each patient and situation is unique. It is our promise to customize the process to each patient‘s individual needs.

PGT-M full disease list

Is PGT-M for you?

This test is recommended if:

You already have a child affected by a genetic disease.
You and your partner are carriers of the same genetic disease.
You or your partner have been diagnosed with a single gene disease or have a family history of a genetic disease.

PGT-M full disease list

How does it work?

What now?

Other services

CGT

Carrier Genetic Test
Determines the risk of having a child with a genetic disease

More information

PGT-A

Improves the chances of reproductive success by selecting chromosomally normal embryos

More information

PGT-A + ERA Synchrony

The best embryo at the right time

More information

Igenomix is in the media

Igenomix is not affiliated with any news outlet or publication identified above. News coverage does not constitute an endorsement of Igenomix or its products.

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

Healthy embryos are selected to be transferred in the IVF process

Performed for >99% of inherited single gene disorders

PGT-M detects more than 300 genetic diseases

What are chromosomes and genes?

What is PGT-M test?

Why use PGT-M?

Is PGT-M for you?

FULL DISEASE LIST

BROCHURE

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What now?

CGT

PGT-A

PGT-A + ERA Synchrony

PGT-M Preimplantation Genetic Testing for Monogenic disorders

If you have an inherited disease, we can help you to have a healthy baby

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

Healthy embryos are selected to be transferred in the IVF process

Performed for >99% of inherited single gene disorders

PGT-M detects more than 300 genetic diseases

What are chromosomes and genes?

What is PGT-M test?

Why use PGT-M?

Is PGT-M for you?

FULL DISEASE LIST

BROCHURE

Subscribe to our newsletter

What now?

Other services

CGT

PGT-A

PGT-A + ERA Synchrony

Igenomix is in the media

Subscribe to
our newsletter