Prenatal Genetic Diagnosis

Diagnosis of many chromosomal or genetic diseases of the baby is based on the principle of taking one or two of the cells of the embryo (baby) formed by one of the in vitro fertilization methods out of its shell and examining it with various methods. Today, all known chromosomal and genetic diseases can be detected with great accuracy before the embryo is placed in the womb, and the healthy embryo can be selected.