The power to decide better
We know that information is necessary to be able to make decisions, but also that too much of it, or if it is presented in a complicated way, can be incomprehensible or overwhelming. For this reason, our team of genetic advisers, whether you are a parent, donor, clinic or medical professional, is at your disposal throughout the process.
The results are in. And now what?
We will send the clinic a detailed and personalized report with the results, so that the gynaecologist and the patient can better plan decision-making in the reproductive process.
When the test result is positive and, therefore, the same pathological variant is detected:
If it is an incompatibility in a positive matching study between the patient and the donor, the donor must be replaced by another compatible one.
If it is a couple, and both are carriers of the same variant that causes disease, the genetic adviser will inform them of the options available to minimise the risk. Tests such as PGT or prenatal tests such as chorionic villus sampling or amniocentesis will be recommended, which could determine if the baby is or will be affected with the recessive disorde.