The Department of Medical Genetics, examined patients referred by physicians of any profile for the diagnosis of hereditary diseases, for the prediction of offspring in families where there was, is, or is expected of patients with hereditary disorders, in order to calculate the risk of having an affected child.

Other category surveyed at geneticists is couples considering as healthy and the relatives, but wishing to be convinced in genetic health of the planned child. Are surveyed both women going to become pregnant, and pregnant women

  In specialized laboratory patients for an exception of chromosomal pathology (with multiple developmental anomalies, deviations in sexual, physical, intellectual development), the married couples having children with a Down syndrome or congenital defects of various bodies, couples with infertility and a pregnancy nevynashivaniye are surveyed. In many cases manifestations of hereditary diseases of a metabolism are a delay of psychological, speech, intellectual development therefore this contingent of patients is surveyed in biochemical laboratory of hereditary diseases.

  In case of detection during research of pathological genes (hemophilia, cystic Fibrosis, fenilketonuriya, adrenogenital sindromoma, muscular dystrophies, amiotrofiya, myopathies, trochees of Gettington and many other diseases), patients receive explanations about percent of genetic risk and manifestations with them connected. After receiving such result only parents resolve an issue to have children or not.

  The list of diagnostic genetic testings is huge. The doctor geneticist makes the decision on carrying out these or those inspections at internal consultation with the woman (couple).

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