Please use this identifier to cite or link to this item: http://repo.knmu.edu.ua/handle/123456789/16930
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dc.contributor.authorPilipenko, Natalia-
dc.contributor.authorRomanova, Natalia-
dc.date.accessioned2017-06-27T06:06:58Z-
dc.date.available2017-06-27T06:06:58Z-
dc.date.issued2017-05-24-
dc.identifier.citationPilipenko N. Mayer-Rokitansky-Kuster-Hauser syndrome (a clinical case) / N. Pilipenko, N. Romanova // Xth International Scientific Interdisciplinary Conference (ISIC) for medical students and young scientists, Ukraine, 24–26 may 2017 : abstract book. – Kharkiv : KhNMU, 2017. – P. 156–157.ru_RU
dc.identifier.urihttps://repo.knmu.edu.ua/handle/123456789/16930-
dc.description.abstractCongenital aplasia of the uterus and vagina occurs from 1 in 5000 to 1 in 20000 among newborn girls. Clinical case. A 16-year-old patient A. was admitted to the Regional Children’s Clinical Hospital No.1 of the Department of Obstetrics, Gynecology and Children's Gynecology on 18.11.2016 with complaints on the absence of menstruation.Clinical diagnosis: Mayer-Rokitansky-Kuster-Hauser syndrome. The patient was recommended to undergo elective surgical treatment. The operation of vaginal grafting with a segment of the sigmoid colon was performed after preoperative preparation, on 30th November, 2016. The postoperative period was uneventfulru_RU
dc.language.isoenru_RU
dc.publisherKhNMUru_RU
dc.subjectMayer-Rokitansky-Kuster-Hauser syndromeru_RU
dc.subjectaplasia of the uterus and vaginaru_RU
dc.subjectoperation of vaginal graftingru_RU
dc.titleMayer-Rokitansky-Kuster-Hauser syndrome (a clinical case)ru_RU
dc.typeThesisru_RU
Appears in Collections:Наукові роботи молодих вчених. Кафедра акушерства, гінекології та дитячої гінекології

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