About PGT
Safe, reliable and personalized care
What it offers:
Preimplantation Genetic Testing (PGT) is an advanced technique that allows embryos to be tested prior to transfer to the uterus. This test helps identify possible genetic or chromosomal abnormalities in the embryos, ensuring that only healthy embryos are selected for transfer.
Recommended option for:
Patients with a history of genetic disorders, recurrent pregnancy loss, or advanced maternal age. It’s also ideal for those undergoing IVF who wish to select the healthiest embryos for transfer, maximizing their chances of a successful and healthy pregnancy.
How it works?
During the IVF process, a small number of cells are carefully biopsied from each embryo on day five or six of development.
These cells are then analyzed in a specialized laboratory to identify chromosomal abnormalities or specific genetic conditions.
The healthiest embryos are selected for transfer, ensuring the best possible outcomes for your family-building journey.
In addition, PGT allows for sex selection of the baby, an option that may be indicated in certain medical cases to avoid gender-specific diseases.
Preimplantation Genetic Testing (PGT)
What Does the PGT method Involve?
1. Embryo Development in the Laboratory
Embryos are created through IVF and cultured in the lab until they reach an early stage of development.
2. Biopsy of Embryos
A few cells are carefully extracted from each embryo without compromising its viability.
3. Genetic Analysis
The extracted cells are analyzed for genetic or chromosomal abnormalities, identifying healthy embryos free from specific conditions.
4. Embryo Selection and Transfer
Genetically normal embryos are selected and transferred to the uterus, improving pregnancy success rates and reducing the risk of miscarriage.
“Empower your journey with knowledge.
Ensure a healthy start for your baby and the possibility to choose the family balance you dream of.”
Benefits
Reduced risk of genetic disease transmission.
Increased pregnancy success rate by transferring only healthy embryos.
Option to select the sex of the baby for specific medical reasons.
Frequently asked questions
PGT is a genetic screening method performed on embryos to detect genetic abnormalities, increasing the chances of a successful pregnancy.
PGT can identify chromosomal abnormalities, inherited genetic disorders, and even help select the embryo’s sex if desired.
Yes, PGT can accurately determine the sex of the embryo, allowing for family balancing if desired.
PGT is an optional add-on for IVF and is recommended for patients with a history of genetic conditions or recurrent pregnancy loss.
Results are typically available within 7-10 days after embryo biopsy.