Preimplantation Genetic Testing (PGT) is a process used in conjunction with in vitro fertilization (IVF) to screen embryos for genetic abnormalities. PGT-M focuses on identifying specific genetic mutations that could be passed on to offspring, while PGT-A assesses the overall chromosomal health of embryos to increase the chances of a successful pregnancy. Both PGT methods help ensure that only the healthiest embryos are selected for implantation, making it a valuable tool for couples undergoing IVF, especially those with known genetic risks or recurrent pregnancy loss.
PGT Process Steps in IVF
Preimplantation Genetic Testing for Aneuploidy (PGT-A), previously known as Preimplantation Genetic Screening (PGS), offers several benefits in the context of in vitro fertilization (IVF). Here are some key advantages:
Overall, PGT-A can be a valuable tool in enhancing the success of IVF, providing hopeful outcomes for many aspiring parents.
Preimplantation Genetic Testing for Monogenic disorders (PGT-M), formerly known as Preimplantation Genetic Diagnosis (PGD), offers several benefits for couples considering in vitro fertilization (IVF) who are at risk of passing on genetic conditions. Here are some key advantages:
Overall, PGT-M offers a proactive approach to managing genetic risks and supports families in achieving their reproductive goals.
If you’ve tried to start a family without success, even with assisted reproductive services, we invite you to speak with our genetic experts at Netcare IVF| Fertility to explore how provides cutting-edge genetic screening and diagnostic services (PGT-M and PGT-A ) specifically designed for in vitro fertilization can help. These techniques screen embryos for genetic abnormalities, allowing our team to identify genetic conditions early and enhancing your chances of achieving a healthy pregnancy and delivering a strong baby. To discover more about the innovative solutions our genetic team offers for infertility, reach out to our team today.
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