Pre-Implantation Genetic Testing (PGT)

Service Description

Pre-Implantation Genetic Testing (PGT) screens embryos for genetic abnormalities before IVF implantation, helping identify healthy embryos and improving pregnancy success while reducing inherited risks. Preimplantation Genetic Testing (PGT) We provide advanced genetic testing with both PGT-A and PGT-M to help ensure the best outcomes for your fertility journey: PGT-A (Aneuploidy): This test evaluates the chromosomal health of embryos by checking for abnormalities such as extra or missing chromosomes. It helps identify the healthiest embryos for transfer, increasing the chances of implantation, reducing the risk of miscarriage, and improving the likelihood of a successful pregnancy. PGT-A is particularly beneficial for patients with a history of recurrent pregnancy loss, older maternal age, or multiple failed IVF cycles. PGT-M (Monogenic Disorders): Designed for couples with a known risk of passing on a specific genetic condition, PGT-M screens embryos for hereditary disorders such as cystic fibrosis or thalassemia. This testing ensures that only embryos free of the targeted condition are selected for transfer, helping to prevent the transmission of genetic diseases and giving families greater peace of mind. Our comprehensive PGT services are tailored to provide the highest level of care and support, empowering you with the knowledge and confidence to move forward on your path to parenthood.