Screening Embryos for Healthier Pregnancies and Healthier Generations
PGT/PGS is a genetic testing method performed during IVF to evaluate embryos for chromosomal abnormalities or inherited conditions. This helps increase pregnancy success rates, reduce the risk of genetic disorders, and empower families with informed decisions before implantation.
Conditions Detected by PGT/PGS
Chromosomal
Aneuploidies
Single-Gene
Disorders
Structural
Rearrangements
Sex Chromosome Abnormalities
Why PGT/PGS is a Game Changer
How Does PGT/PGS Work?
A quick and precise genetic screening during IVF embryo development.
Embryo Biopsy
A few cells are carefully removed from the embryo on day 5 or 6.
Genetic Analysis
Cells are analyzed in our advanced lab for chromosomal or genetic conditions.
Embryo Selection
Only healthy embryos are chosen for implantation, enhancing IVF success.
Why Choose FSG for PGT/PGS
Advanced
Screening
We use comprehensive PGT-A and PGT-M panels for detailed embryo analysis.
IVF
Collaboration
Seamless integration with IVF clinics to ensure safe and effective testing.
Fast Reporting
Receive results in just a few days to support timely embryo transfer.
Trusted
Genetics Lab
FSG is a UAE-certified genomics leader with a reputation for accuracy and care.
Frequently Asked
Questions!
We’re here to help. Explore answers or reach out to our team directly.
PGT/PGS is a procedure used during IVF to screen embryos for genetic abnormalities before implantation. It helps identify healthy embryos, increasing the chances of a successful pregnancy.
It is often recommended for couples with a history of genetic disorders, recurrent miscarriages, advanced maternal age, or previous failed IVF attempts.
Yes, the biopsy is done at a stage where it does not harm the embryo’s development. It is performed by highly trained specialists using advanced techniques.
PGT can detect chromosomal abnormalities (like Down syndrome) and specific inherited genetic disorders, depending on the test type (PGT-A, PGT-M, or PGT-SR).
While it significantly reduces the risk of genetic issues, it cannot guarantee a completely healthy baby. It improves the likelihood of a successful and healthy pregnancy.
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