- Two Cases of Congenital Vaginal Absence
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Sung Chul Park, Hyun Jin Shin, Hyo Hyun Kim, Tae Hyung Lee, Sung Ho Lee, Doo Jin Lee
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Yeungnam Univ J Med. 2007;24(2 Suppl):S710-718. Published online December 31, 2007
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DOI: https://doi.org/10.12701/yujm.2007.24.2S.S710
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 Abstract
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- Congenital absence of vagina(Mayer-Rokitansky-Küster-Hauser syndrome) is found between 1 in 4,000 and 20,000 female births, and is frequently associated with various urinary tract and skeletal anomalies. As the patients have normal ovarian functions, they appear as normal female phenotype and have normal female karyotype 46, XX. Inability of coitus is one of the main problems they have, so the goal of treatment is to create a vagina adequate to allow sexual activity. Both surgical and nonsurgical approaches have been utilized. The authors experienced two cases of congenital absence of vagina successfully treated by surgical and nonsurgical method.
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Yeungnam University College of Medicine
