Full-thickness skin graft colpopoiesis in the patient with the mayer-rokitansky-kuster syndrome: a case report

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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.

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 Petersburg

М. 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 Petersburg

Е. 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

References


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