Mayer-Rokitansky-Küster-Hauser syndrome associated with a urogenital sinus anomaly in a 4-year-old : report of a case

dc.contributor.authorAdam, Ahmed
dc.contributor.authorEbrahim, Zaeem I.
dc.contributor.authorEngelbrecht, Matthys J.
dc.contributor.authorVan Heerden, Izak J.
dc.contributor.authorMoshokoa, Evelyn M.
dc.date.accessioned2010-11-09T09:37:55Z
dc.date.available2010-11-09T09:37:55Z
dc.date.issued2009
dc.description.abstractThe 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.citationAdam, 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.issn1661-7649
dc.identifier.other10.1159/000189693
dc.identifier.urihttp://hdl.handle.net/2263/15230
dc.language.isoenen_US
dc.publisherKargeren_US
dc.rightsKargeren_US
dc.subjectMayer-Rokitansky-Küster-Hauser syndromeen_US
dc.subjectUrogenital sinus anomalyen_US
dc.titleMayer-Rokitansky-Küster-Hauser syndrome associated with a urogenital sinus anomaly in a 4-year-old : report of a caseen_US
dc.typePostprint Articleen_US

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