dc.contributor.author | Adam, Ahmed | |
dc.contributor.author | Ebrahim, Zaeem I. | |
dc.contributor.author | Engelbrecht, Matthys J. | |
dc.contributor.author | Van Heerden, Izak J. | |
dc.contributor.author | Moshokoa, Evelyn M. | |
dc.date.accessioned | 2010-11-09T09:37:55Z | |
dc.date.available | 2010-11-09T09:37:55Z | |
dc.date.issued | 2009 | |
dc.description.abstract | The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare entity characterized by congenital aplasia of the vagina and uterus in the presence of normal ovarian function, in conjunction with a 46 XX karyotype. This condition is mostly signalled by primary amenorrhoea around the season of puberty. We report on its diagnosis in a 4-year-old child presenting with urinary incontinence. Also of interest in our index patient is the presence of a pure urogenital sinus anomaly. This extremely rare association has not been previously diagnosed in childhood. | en_US |
dc.identifier.citation | Adam, A, Ebrahim, ZI, Engelbrecht, MJ, Van Heerden, IJ & Moshokoa, EM 2009, 'Mayer-Rokitansky-Küster-Hauser syndrome associated with a urogenital sinus anomaly in a 4-year-old : report of a case', Current Urology, vol. 3, no. 2, pp. 103-105. [http://content.karger.com/ProdukteDB/produkte.asp?Aktion=JournalHome&ProduktNr=231997] | en_US |
dc.identifier.issn | 1661-7649 | |
dc.identifier.other | 10.1159/000189693 | |
dc.identifier.uri | http://hdl.handle.net/2263/15230 | |
dc.language.iso | en | en_US |
dc.publisher | Karger | en_US |
dc.rights | Karger | en_US |
dc.subject | Mayer-Rokitansky-Küster-Hauser syndrome | en_US |
dc.subject | Urogenital sinus anomaly | en_US |
dc.title | Mayer-Rokitansky-Küster-Hauser syndrome associated with a urogenital sinus anomaly in a 4-year-old : report of a case | en_US |
dc.type | Postprint Article | en_US |