is one of the rarest anomalies of the vaginal tract, it is estimated that only one out of every 70,000 women is presented. It is a congenital malformation of unknown cause. Divides the vagina into two segments and partially or completely blocked the exit of menstrual flow and vaginal and therefore is detectable at puberty because it causes amenorrhea and cyclic pelvic pain and blood retention and bloating of the bodies . It must intervene urgently to be detected, because it can cause total loss of the organ, which would need to create another 'vagina' from a dissection of the space between the bladder and rectum. In the new site introduces a vaginal mold by adding a skin graft (known as Mclndoe operation).
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