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Aim. To estimate the importance of the main screening programs for congenital and hereditary diseases (CHD) in pregnant women, fetus and newborns. Material and methods. The analysis of screenings results of early CHD diagnostics in the prenatal, perinatal and neonatal periods is carried out. The assessment of the main indicators of work and activity of the medical organizations for CHD diagnostics is given. When carrying out the analysis of indicators data of ROSSTAT (Federal Statistics) of the Russian Federation and Tatarstanstat (Local Statistics) were used. Results and discussion. Efficiency of the screening programs directed on earlier detection of congenital and hereditary pathology is noted. Growth of incidence and decrease in infantile mortality on a class of diseases: congenital anomalies (malformations), deformation and chromosomal violations is established. The model of arrangement of tasks in service of obstetric aid and the childhood directed on timely diagnostics and preservation of health of the children's population is created. Congenital defects screening programs promotes its early identification, optimum treatment,

vestnik sovremennoj kliničeskoj mediciny

Early diagnosis of congenital pathology as a significant reserve of decrease in incidence and mortality of the population (experience of the Republic of Tatarstan)