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¿µ³²ÀÇ´ëÇмúÁö Vol.24_No.2 Suppl. P.S710-718, Dec. 2007

Case Report

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Two Cases of Congenital Vaginal Absence

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Tel: (053) 620-3435. Fax: (053) 654-0676
E-mail: djlee@med.yu.ac.kr.

December 30, 2007

Abstract

Congenital absence of vagina(Mayer-Rokitansky-Kuster-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.

Key Words: Congenital absence of vagina, Ingram method, McIndoe operation

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