The features of the course of pregnancy and the outcomes of labor during cystinuria


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅或者付费存取

详细

Background. Cystinuria is an autosomal recessive hereditary disease associated with impaired transport of dibasic amino acids (including cystine) and with the formation of coral renal calculi, which is accompanied by frequent surgical interventions and recurrent pyelonephritis. Case report. A primigravida patient was hospitalized for a period of29-30 weeks with an exacerbation of chronic pyelonephritis of only one right working kidney. Combination treatment made it possible to prolong pregnancy up to 34 weeks. Early delivery is due to signs of renal failure. Conclusion. Strict adherence to the rules of management of pregnant women with only one working kidney in the presence of chronic pyelonephritis could delay delivery to an optimal period in terms of minimizing perinatal complications.

全文:

受限制的访问

作者简介

Alexander Strizhakov

I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University)

Email: kafedra-agp@mail.ru
MD, academician of the Russian Academy of Sciences, professor, head of the Department of Obstetrics, Gynecology and Perinatology of the Faculty of Medicine

Irina Bogomazova

I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University)

Email: kafedra-agp@mail.ru
PhD, associate Professor of the Department of Obstetrics, Gynecology and Perinatology of the Faculty of Medicine

Irina Ignatko

I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University)

Email: iradocent@mail.ru
MD, corresponding member of the Russian Academy of Sciences, professor of the Russian Academy of Sciences, professor of the Department of Obstetrics, Gynecology and Perinatology of the Faculty of Medicine

Vera Belousova

I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University)

Email: kafedra-agp@mail.ru
PhD, associate professor, associate professor of the Department of Obstetrics, Gynecology and Perinatology of the Faculty of Medicine

Elena Timokhina

I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University)

Email: kafedra-agp@mail.ru
MD, associate professor, professor of the Department of Obstetrics, Gynecology and Perinatology of the Faculty of Medicine

Madina Kardanova

I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University)

Email: kafedra-agp@mail.ru
PhD, assistant professor of the Department of Obstetrics, Gynecology and Perinatology of the Faculty of Medicine

Anton Kuznetsov

I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University)

Email: kafedra-agp@mail.ru
post-graduate student of the Department of Obstetrics, Gynecology and Perinatology of the Faculty of Medicine

Natalia Afanasyeva

S.S. Yudin City Clinical Hospital, Moscow Healthcare Department

Email: gkb-yudina@zdrav.mos.ru
PhD, deputy chief physician for obstetrics and gynecology

Yulia Samoilova

S.S. Yudin City Clinical Hospital, Moscow Healthcare Department

Email: gkb-yudina@zdrav.mos.ru
PhD, head of the Department of Pregnancy Pathology of maternity hospital

参考

  1. Koulivand L., Mohammadi M., Ezatpour B., Salehi R., Markazi S., Dashti S., Kheirollahi M. Mutation analysis of SLC3A1 and SLC7A9 genes in patients with cystinuria. Iran. J. Kidney Dis. 2015; 43(5): 447-53.
  2. Cannizzo S.A., Stinner M., Kennedy-Stoskopf S. Prevalebce of cystinuria in servals (leptailurus serval) in the United States. J. Zoo Wildl. Med. 2017; 48(4): 1102-7.
  3. Krishnamurthy S., Pavani C., Kurup P.M., Palanisamy S., Jagadeesh A., Sekar K. et al. Cystinuria in a 13-month-old girl with absence of mutations in the SLC3A1 and SLC7A9 genes. Indian J. Nephrol. 2018; 28(1): 84-5.
  4. Biyani C.S., Cartledge J.J. Cystinuria - diagnosis and management. EAU-EBU Update Series. 2006; 4(5): 175-83.
  5. Chabrol B., Martens K., Meulemans S., Cano A., Jaeken J., Matthijs G., Creemers J.W. Deletion of C2orf34, PREPL and SLC3A1 causes atypical hypotonia-cystinuria syndrome. J. Med. Genet. 2008; 45(5): 314-8.
  6. Vasudevan V., Samson P., Smith AD., Okeke Z. The genetic framework for development of nephrolithiasis. Asian J. Urol. 2017; 4(1): 18-26.
  7. Reinstatler L., Stern K., Batter H., Scotland K.B., Ardekani G.S., Rivera M. et al. Conversion from cystine to non-cystine stones: incidence and associated factors. J. Urol. 2018; 200(6): 1285-9.
  8. Santos F.M.D., Peres A.K., Mandotti M.R., Peres L.A.B. Metabolic investigation in patients with nephrolithiasis. Einstein (Sao Paulo, Brazil). 2017; 15(4): 452-6.
  9. Mikhaylenko D.S., Prosyannikov M.Y., Baranova A., Nemtsova M.V. Genetic and biochemical features of the monogenic hereditary urolithiasis. Biomed. Khim. 2018; 64(4): 315-25.
  10. Usawachintachit M., Sherer B., Hudnall M., Tzou D.T., Taguchi K., Hsi R.S. et al. Clinical outcomes for cystinuria patients with unilateral versus bilateral cystine stone disease. J. Endourol. 2018; 32(2): 148-53.
  11. Kogturk S., Oktay G., Guner G., Pekgetin C., Gure A. Effect of D-penicillamine on rat lung elastin cross-linking during the perinatal period. Cell Biochem. Funct. 2006; 24(2): 167-72.
  12. Савельева Г.М., Сухих Г.Т., Серов В.Н., Радзинский В.Е., ред. Акушерство. Национальное руководство. 2-е изд. М.: ГЭОТАР-Медиа; 2015.
  13. Mishra V.V., Mistry K.M., Nanda S.S., Choudhary S., Aggarwal R., Gandhi K. Pregnancy outcome in patients with solitary kidney. J. Obstet. Gynaecol. India. 2017; 67(3): 168-72.
  14. Шехтман М.М. Руководство по экстрагенитальной патологии у беременных. 3-е изд. М.: Триада-Х; 2005.
  15. Никольская И.Г., Новикова С.В., Будыкина Т.С., Цивцивадзе Е.Б., Микаелян А.В., Егорова Н.В. Беременность у пациенток с хронической почечной недостаточностью: тактика ведения и родоразрешения при консервативно-курабельной стадии. Российский вестник акушера-гинеколога. 2012; 21(6): 21-8

补充文件

附件文件
动作
1. JATS XML

版权所有 © Bionika Media, 2019