CGT is an advanced carrier genetic test before pregnancy, which determines whether a couple is a carrier of genetic mutations that could be transmitted to their children.
It analyses more than 6,600 mutations associated with over 600 genetic disorders such as Alpha Thalassemia, Glycine encephalopathy, Familial mediterranean fever, Haemochromatosis, Polycystic kidney disease amongst others by NGS.
Results in 20 working days
The tested person carries a mutation in a particular gene. The test should be carried out in the other member of the couple.
A negative result indicates that the person doesn’t carry any of the mutations studied.
There is still a small risk of carrying another mutation not analyzed by the test.