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Obstetrics & Gynecology Science ; : 367-370, 2019.
Article in English | WPRIM | ID: wpr-760656

ABSTRACT

Currarino syndrome is a hereditary disease characterized by the triad of sacral agenesis, anorectal malformation, and presacral mass. Most patients are diagnosed in childhood, and this condition rarely manifests in adulthood. In women, gynecological malformations associated with Currarino syndrome have been reported, such as bicornuate uterus, rectovaginal fistula, and septate uterus. We present a rare case of a 29-year-old woman with a suspected pelvic mass who was diagnosed with Currarino syndrome.


Subject(s)
Adult , Female , Humans , Genetic Diseases, Inborn , Rectovaginal Fistula , Uterus
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