PGT-M of monogenic diseases in 1 – 5 embryos using karyomapping (aneuploidy tested simultaneously)

Testing to rule out the presence of a genetically caused disease in the embryo using the karyomapping method in case the disease runs in the family, or when carriage of the disease has been proven in one or both of the parents. Before treatment, it is necessary to consult a geneticist about the possibilities of diagnosing the disease.

Of which the advance before the start of the IVF cycle – testing of disease carriers: €700