Ureteral switch for bilateral ureteropelvic junction obstruction in a case of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part of the vagina. Secondary sexual characteristics and karyotype are normal. This syndrome affects at least 1 out of 4500 women. MRKH may be isolated (type I) but it is more frequently...

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Bibliographic Details
Main Authors: L.E. Mubenga, J. Lambertz, A Feyaerts, P Van Cangh, F.X. Wese
Format: Article
Language:English
Published: SpringerOpen 2013-12-01
Series:African Journal of Urology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1110570413000787