Answer from: Raúl Olivares, MD
With the PGS, we currently gather 3 different pieces of information about the embryo quality depending on the indication for the PGS. The first one is that we can confirm that the embryo has a normal amount of chromosomes with no structural abnormalities. This is the information we get from the PGT-A, we can also confirm that in cases in which the patients are known healthy carriers of mutations that can cause diseases in the baby like cystic fibrosis or thalassemia.
We can also confirm that the embryos are healthy carriers or free of the disease discarding those embryos that are going to be affected by this single gene-disease. This is done by the PGT-M, and we can also confirm that the embryos are healthy in cases in which patients have translocations, which means that they have exchanged parts of the chromosomes that can be balanced or imbalanced. If they are imbalanced, it can cause problems with the babies.
With the PGT-SR, we can confirm that the embryos are healthy or that they carry this completely balanced translocation, and it’s not going to affect the health of the baby.
Answer from: Solvita Funka, MD
PGD can help in a situation where you have genetic problems in your family, or your age is advanced, also if the sperm quality is poor. PGD will give you more information about your possible embryo. If you had a miscarriage more than once before or in situations when you have IVF procedures once or twice before, and you haven’t achieved a pregnancy in the end, PGD can help as well.
What can we know from PGS test results?
What genetic testing can tell you about the embryo? Who can benefit from PGS testing? When should it be indicated?