Genetic Clarity,
Healthier Beginnings,
Confident Parenthood
Genetic Clarity,
Healthier Beginnings,
Confident Parenthood
PGT (Preimplantation Genetic Testing)
Healthy Embryos. Trusted Surrogacy. Strong Beginnings.
PGT surrogacy combines preimplantation genetic testing with gestational surrogacy to help intended parents achieve a healthy pregnancy. PGT is performed during IVF to screen embryos for genetic or chromosomal abnormalities before implantation. Only healthy embryos are transferred to the surrogate, improving success rates and reducing the risk of inherited disorders. This advanced process offers peace of mind for families with genetic concerns. Together, PGT and surrogacy offer a powerful, hope-filled path to parenthood for individuals or couples facing fertility, medical, or hereditary challenges.
Step By Step Process
Screening Embryos. Ensuring Health. Securing Parenthood.
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Genetic Consultation & IVF Planning :
Intended parents consult fertility specialists to assess genetic risks. IVF is planned, and PGT is recommended if there’s a history of genetic or chromosomal disorders. -
Egg Retrieval & Fertilization :
Eggs are retrieved from the intended mother or donor and fertilized with sperm. Embryos begin to develop in the laboratory under close monitoring. -
PGT Screening of Embryos :
Embryos are biopsied and tested for chromosomal or genetic abnormalities. Only healthy, viable embryos are selected for transfer, increasing chances of a successful, healthy pregnancy. -
Surrogate Preparation & Embryo Transfer :
The surrogate undergoes hormonal preparation. A healthy embryo is then transferred into her uterus in a clinical setting, guided by ultrasound for optimal placement. -
Pregnancy Monitoring & Delivery :
The surrogate’s pregnancy is monitored through regular prenatal care. Upon delivery, the baby is united with the intended parents, fulfilling their dream of a healthy family.
FAQS
Screens embryos during IVF to select genetically healthy ones
Couples with a history of genetic disorders, recurrent miscarriages, or advanced maternal age benefit from PGT to improve embryo selection and increase the chances of a healthy pregnancy.
PGT can identify chromosomal abnormalities (like Down syndrome), single-gene disorders (like cystic fibrosis), and structural rearrangements, helping prevent transmission of serious inherited conditions to the child.
A few cells are gently removed from a day 5 or 6 embryo (blastocyst stage) without harming development, and sent to a lab for genetic analysis.
When performed by experienced specialists, PGT is safe and does not harm the embryo. It often improves implantation rates by selecting only genetically healthy embryos for transfer.
If no viable embryos remain, your doctor may suggest another IVF cycle, donor gametes, or additional testing based on your unique fertility and genetic profile.
Only chromosomally normal embryos are chosen for transfer, increasing the chances of implantation, reducing miscarriage risk, and supporting the goal of a healthy, full-term pregnancy.