TREATMENTS
Preimplantation Genetic Testing
Early Detection of Issues
Identifies chromosomal or genetic conditions before embryo transfer.
Improved Success Rates
Increases chances of a healthy pregnancy with selected embryos.
Peace of Mind for Parents
Reduces the risk of passing on inherited disorders.
About the treatment
Preimplantation Genetic Testing in Cyprus allows embryos created through IVF to be screened for specific genetic or chromosomal abnormalities before transfer. This ensures that only healthy embryos are selected, improving the likelihood of a successful pregnancy and reducing the risk of miscarriage or inherited conditions.

Is PGT right for you?
Are over 35 and concerned about age-related chromosomal risks
Have experienced recurrent pregnancy loss or failed IVF attempts
Carriers of known genetic disorder and wish to avoid passing it on
Have a family history of inherited conditions
Have chromosome rearrangements that may affect embryo health
How PGT Works
Embryo Creation
Eggs and sperm are combined through IVF to create embryos for testing.
Embryo Culture
Embryos are grown in the lab until the blastocyst stage (Day 5/6)
Embryo Biopsy
A few cells are gently taken from the embryo’s outer layer for analysis.
Genetic Test
Examination of cells forchromosomal, genetic abnormalities.
Embryo Transfer
A healthy embryo is selected and transferred to the uterus.
PGT
Types of Genetic Testing
PGT-A
Preimplantation Genetic Testing for Aneuploidies (PGT-A) screens embryos for chromosomal abnormalities. It helps select embryos with the best chance of healthy development, often recommended for women over 35 or those with recurrent pregnancy loss.
PGT-M
Preimplantation Genetic Testing for Monogenic disorders (PGT-M) is used when one or both parents carry a single-gene condition. It ensures embryos without the disorder are chosen, reducing the risk of passing it on to future children.
PGT-S
Preimplantation Genetic Testing for Structural rearrangements (PGT-S) identifies unbalanced chromosome rearrangements in embryos. It is recommended for parents who carry translocations or similar changes, helping prevent affected pregnancies.
Frequently asked Questions
