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Preimplantation Genetic Testing (PGT), previously known as PGS/PGD, is an advanced technique used during IVF to screen embryos for genetic or chromosomal abnormalities before transfer.
A few cells are carefully analyzed from the embryo to identify healthy, chromosomally normal embryos, helping improve implantation success and reduce the risk of genetic disorders or miscarriage.
PGT is recommended for patients with specific genetic or fertility concerns.
Preimplantation Genetic Testing helps improve pregnancy outcomes by ensuring the transfer of chromosomally normal embryos with higher implantation potential and reduced risks.
Increases the chances of successful embryo implantation by selecting genetically normal embryos that are more likely to attach and develop properly.
Helps reduce the risk of miscarriage by avoiding the transfer of embryos with chromosomal abnormalities that may affect pregnancy progression.
Supports the development of a healthy pregnancy by ensuring only genetically screened embryos with normal chromosomal patterns are selected for transfer.
It is a genetic testing technique used to screen embryos before implantation during IVF.
PGT is an additional step within IVF to assess embryo genetics before transfer.
Yes, it is a safe and widely used laboratory procedure when performed by experts.
Couples with genetic risks, repeated IVF failures, or recurrent miscarriages.
It improves success rates but does not guarantee pregnancy.
It helps identify embryos without specific genetic abnormalities.
Testing is performed on selected embryos based on clinical indication.
It is advised after evaluation based on medical and genetic factors.
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