Value of genetic testing of herminal tumor mutations in screening and prevention of malignant formations
Abstract
The authors analyzed available data in modern literature on the role of genetic testing for mutations in genes responsible for predisposing to hereditary cancers of reproductive organs in women. They are looking at data on the importance of using genetic testing in clinical practice to predict the disease development, need for follow-up monitoring in the presence of mutation load, and determination of combined chemotherapy policy for malignant neoplasms.
About the Authors
O. A. Buyanovskaya
National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Россия
O. V. Burmenskaya
National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Россия
А. . Goltsov
National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Россия
T. . Kochetkova
National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Россия
J. . Shubina
National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Россия
N. . Mishina
National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Россия
D. Yu. Trofimov
National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Россия
For citations:
Buyanovskaya O.A.,
Burmenskaya O.V.,
Goltsov А.,
Kochetkova T.,
Shubina J.,
Mishina N.,
Trofimov D.Yu.
Value of genetic testing of herminal tumor mutations in screening and prevention of malignant formations. Medical Genetics. 2020;19(6):40-41.
(In Russ.)
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