DOI: 10.36347/sjams.2018.v06i10.012

Pages: 3725-3729

Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH) is a rare entity which includes a set of deformations of the feminine genital tract and the internal reproductivs organs. The surgical treatment aims at restoring at the most the vagina to make possible sexuality but the function of reproduction remains limited. We describe a case of 24 year old patient who consults the day after its wedding night for imperforation of the hymen. And to whom we discover a syndrome of rokytansky type1 with vaginal total agenesis and hypoplasic uterus and ovary. The creation of a neovagina was impossible