Журнал включен в российские и международные библиотечные и реферативные базы данных
РИНЦ (Россия)
RINZ (RUSSIA)
Регистрационное агентство DOI (США)
DOI Registration Agency (USA)
Эко-Вектор (Россия)
Eco-Vector (Russia)
Ulrichsweb (Ulrich’s Periodicals Director

Prevention of hereditary and congenital diseases of the kidneys and urinary tract

DOI: https://doi.org/10.29296/25879979-2021-05-06
Download full text PDF
Issue: 
5
Year: 
2021

K.I. Grigoriev, O.F. Vykhristyuk, A.L. Solovyova, E.E. Vartapetova, N.I. Pirogov Russian National Research Medical University, Russian Health Ministry

Interest in the problem of hereditary and congenital diseases of the kidneys and urinary tract in children is under constant attention of specialists, which is associated with an increase in the possibility of diagnosis and the growth of chronic kidney diseases, a serious basis of which they constitute. A review of modern domestic and foreign periodicals about hereditary and congenital diseases of the kidneys and urinary tract, in most cases the latent nature of their course, is presented. Various nosological forms of diseases are considered. The emphasis is on the modern possibilities of medical and genetic counseling, primary prevention of hereditary and congenital diseases of the kidneys and urinary tract in pediatric practice, and their timely diagnosis.

Keywords: 
children
hereditary and congenital diseases of the kidneys and urinary tract
prevention
nursing control



It appears your Web browser is not configured to display PDF files. Download adobe Acrobat или click here to download the PDF file.

References: 
  1. Vjalkova A.A., Zorin I.V., Chesnokova S.A., Plotnikova S.V. Rannjaja diagnostika hronicheskoj bolezni pochek u detej. Nefrologija. 2019. t. 23. №5: 135-137.
  2. Detskaja nefrologija. Pod red. P.V. Shumilova, E.K. Petrosjan, O.L. Chugunovoj. M.: MEDPRESS-inform, 2018, 500 s.
  3. Detskaja nefrologija / pod red. E. Lojmanna, A.N. Tsygina, A.A. Sarkisjana. M.: Litterra, 2010, 400 s.
  4. Dlin V.V., Ignatova M.S., Kon'kova N.E. Klinicheskie rekomendatsii po diagnostike i lecheniju sindroma Al'porta u detej. Nefrologija. 2015. t. 19. №3: 86-89.
  5. Ignatova M.S., Dlin V.V. Nasledstvennye zabolevanija pochek, protekajuschie s gematuriej. Ros vestnik perinatol i pediatr. 2014. № 3: 82-88.
  6. Kutyrlo I.E., Savenkova N.D. CAKUT – sindrom u detej. Nefrologija. 2017; 21(3):18-24. https://doi.org/10.24884/1561-6274-2017-3-18-24
  7. Leviashvili Zh.G, Savenkova N.D, Anichkova I.V. Osobennosti patologii pochek u detej s Lowe sindromom. Nefrologija. 2015; t. 19. № 6: 53-60
  8. Movchan E.A., Manakova Ja.L., Galkina E.A., Telegina T.A. Sindrom schelkunchika v nefrologicheskoj praktike. Klinicheskaja nefrologija. 2019. № 2: 44-48.
  9. Osmanov I.M. Mochekamennaja bolezn'. Detskaja nefrologija. Pod red. M.S. Ignatovoj. M: MIA, 2011: 439–456.
  10. Prihodina L.S., Zaharova I.N. Progressirovanie zabolevanij pochek u detej: patogenez, faktory riska, terapija. M.: RMANPO, 2019. – 77 s
  11. Chugunova O.L., Cherkasova S.V., Tumanova E.L., Shumilov P.V., Glashkina S.A., Kyshtymov M.V., Voronina E.F., Grebenkina E.Ju. Polikistoznaja bolezn' pochek u novorozhdennyh i detej rannego vozrasta: problemy diagnostiki, vedenija i lechenija. Pediatrija. 2015. № 3: 99-91.
  12. Moreva G., Elfimov D., Luk'janova V., Elfimova I. Formirovanie kontseptsii hronicheskoj bolezni pochek i ee vnedrenie v pediatricheskuju praktiku. Vrach, 2017; (8): 32-36
  13. Jarovoj S., Guseva N., Rojuk R.. Vlijanie soputstvujuschih zabolevanij na vybor antibakterial'noj terapii pielonefrita. Vrach, 2019; (8): 17-24 https://doi.org/10.29296/25877305-2019-08-04
  14. Deljagin V., Ismailova I., Gorbylev P. Diagnostika infektsii mochevyvodjaschih putej u grudnyh detej. Vrach, 2017; (8): 78-80
  15. Sharshatkin A.V., Mojsjuk Ja.G., Sushkov A.I., Kvadratova N.G. i dr. 25-letnij opyt transplantatsii pochki detjam. Vestnik transplantologii i iskusstvennyh organov. 2016. T.18. №5: 122-127.
  16. Jur'eva E.A., Dlin V.V., Kudin M.V., Novikova N.N., Vozdvizhenskaja E.S., Harabadze M.N., Knjazev Obmennye nefropatii u detej: prichiny razvitija, kliniko-laboratornye projavlenija. Ros. vestnik perinatol. i pediatr 2016. № 2: 28-32.
  17. Vergman C. ARPKD and early manifestations of ADPKD: the original polycystic kidney disease and phenocopies. Pediatric Nephrology. 2015; 30 (1): 15–30.
  18. Bulum B, Ozcakar ZB, Ustuner E, Dusunceli E, Kavaz A, Duman D, et al. High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT. Pediatr Nephrol 2013; 28 (11): 2143–2147.
  19. Renkema KJ, Winpred PJ, Scovorodkin IN et al. Perspectives for understanding congenital anomalies of the kidney and urinary tract (CAKUT). Nephrol Dial Transplant Dec., 2011; 26(14): 3841-3851
  20. Rheault M.N., Kren S.M., Hartich L.A. X-inactivation modifies disease severity in female carriers of murine X-linked Alport syndrome. Nephrol.Dial. Transp. 2010;25: 764-769.
  21. Torra R, Furlano M. New therapeutic options for Alport syndrome. Nephrol Dial Transplant. 2019;34(8):1272–9. https://doi.org/10.1093/ndt/gfz131.
  22. Zhang L., Sun B., Zhao B., Ma Q. An overview of the multi-pronged approach in the diagnosis of Alport syndrome for 22 children in Northeast China. BMC Nephrology (2020) 21:294-299.