What Is PGT (Genetic Testing)?
PGT (preimplantation genetic testing/diagnosis) is the genetic examination of embryos before they are transferred to the uterus. A few cells taken from the embryo at the blastocyst stage are analysed to identify chromosomally healthy embryos.
PGT-A screens for chromosome number abnormalities (aneuploidy); it is recommended in advanced maternal age, recurrent miscarriage and recurrent IVF failure. PGT-M, on the other hand, allows a healthy embryo to be selected where a single-gene disease is known in the family (such as SMA, thalassaemia or cystic fibrosis).
Transferring a healthy embryo increases the pregnancy rate, reduces the risk of miscarriage and raises the chance of a healthy birth. At Clavis IVF Center, PGT is carried out safely by our experienced embryology team with blastocyst biopsy. You can see our PGT treatment page for details.
Key Points
- Chromosome analysis before transfer
- PGT-A: numerical abnormalities; PGT-M: single-gene diseases
- Recommended in advanced age and recurrent losses
- Reduces miscarriage risk, improves success
About PGT (Genetic Testing)
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