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 Beta Thalassemia, Spinal Muscular Atrophy, Sickle Cell, Hemophilia A, DMD, Fragile X among others by NGS.
Most carriers of genetic mutations don’t have a family history of these disorders.
Results in 30 working days
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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.