Abstract
Five cases of double uterus associated with unilateral renal agenesis and ipsilateral blind vagina are presented. The patients complained of chronic or recurrent, fetid vaginal secretion. One of the patients was diagnosed at 4 years of age. Laparotomy revealed the presence of an atretic ureter or wolffian duct remnants in 4 cases; a communication with the blind vagina was present in 3.
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