GENETIC TESTING
Provide preimplantation genetic testing to ensure embryo health and increase the chances of a healthy baby.
PGT-M
PGT-A
What is it?
PGT
PGT
Preimplantation Genetic Testing (PGT) is an examination of embryos for specific genetic abnormalities before their transfer to the uterus during the IVF procedure. The purpose of this testing is to maximize the chance of having a healthy child for parents at high risk of passing on a hereditary disease. This type of testing eliminates the possibility of transmitting the disease to the child.
Types of
PGT
PGT
PGT-M
Preimplantation Genetic Testing for Monogenic Diseases (PGT-M) involves the examination of embryos for specific gene mutations (a particular monogenic disorder) before their implantation in the uterus. This kind of testing virtually eliminates the risk of parents passing on the disease to their child or the birth of a child with a severe illness.
01
PGT-A
PGT-A involves the genetic assessment of embryos to determine whether they have the correct number of chromosomes. Aneuploidy refers to an abnormal number of chromosomes, which can lead to implantation failure, miscarriage, or genetic disorders in the offspring.
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