Full-thickness skin graft colpopoiesis in the patient with the mayer-rokitansky-kuster syndrome: a case report
- Authors: Izmailov R.М.1, Korshunov М.Y.1, Sazykina Е.I.2, Kaplan Е.V.3
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Affiliations:
- Saint Petersburg State Medical University named after I.I. acad. I.P. Pavlova
- Vsevolozhsk central regional hospital
- Center for Pelvic Medicine and Advanced Technologies in Gynecological Surgery
- Issue: Vol 54, No 5S (2005)
- Pages: 99-99
- Section: Reviews
- URL: https://journals.rcsi.science/jowd/article/view/87599
- DOI: https://doi.org/10.17816/JOWD87599
- ID: 87599
Cite item
Abstract
Introductions. The congenital absence of the vagina has a low incidence but it is a very invalidating condition. The Mayer-Rokitansky-Kuster syndrome represents 90% of all cases of vaginal aplasia.
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##article.viewOnOriginalSite##About the authors
R. М. Izmailov
Saint Petersburg State Medical University named after I.I. acad. I.P. Pavlova
Author for correspondence.
Email: info@eco-vector.com
Candidate of Medical Sciences, Ultrasound Diagnostician, Department of Obstetrics and Gynecology
Russian Federation, Saint PetersburgМ. Y. Korshunov
Saint Petersburg State Medical University named after I.I. acad. I.P. Pavlova
Email: info@eco-vector.com
Doctor of Medical Sciences, Associate Professor of the Department of Obstetrics, Gynecology and Reproductology
Russian Federation, Saint PetersburgЕ. I. Sazykina
Vsevolozhsk central regional hospital
Email: info@eco-vector.com
Russian Federation, Vsevolozhsk
Е. V. Kaplan
Center for Pelvic Medicine and Advanced Technologies in Gynecological Surgery
Email: info@eco-vector.com
Russian Federation, San Francisco