The study of immunogenetic markers associated with the development of complications of pregnancy and perinatal pathology in newborns is of great practical importance for the development of preventive measures and maintaining the health of the baby in the future. Numerous studies in recent years have shown that the presence of genetic predisposition to certain diseases is associated with an increased risk of pregnancy complications (habitual miscarriage, placental insufficiency, late toxicosis), which leads to the implementation of perinatal pathology in later life.

There is a system of genetic consultation, which includes diagnostics, defining the type of heredity and prognosis for family. Genetic consultation must help in 8-10% of all families. The staff on MGC consists in clinical genetic, cytogenetic, pediatrician, gynaecologist and other specialists. The main task of genetic consultation is prevention of hereditary diseases.