PGT-M of selected monogenic diseases using the OneGenePGT method – up to 5 embryos

Vylúčenie prítomnosti geneticky viazaného ochorenia metódou NGS u embrya v prípade, ak sa toto ochorenie Testing to rule out the presence of a genetically caused disease in the embryo using the NGS 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. This method can be used to diagnose mutations in sickle cell disease, BRCA 1 and 2 mutations, cystic fibrosis gene mutations, Huntington’s disease gene mutations, and to rule out the fragile X chromosome.