A Case of Complete Testicular Feminization Syndrome.

Moon, T S; Rho, J S; Park, J H; Jeon, D J; Jang, Y W; Koo, J N; Park, Y S; Woo, Y J; Kim, H S

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Case Report

Korean Journal of Obstetrics & Gynecology 1999;42(7):1599-1603.
Published online January 1, 2001.

A Case of Complete Testicular Feminization Syndrome.

T S Moon, J S Rho, J H Park, D J Jeon, Y W Jang, J N Koo, Y S Park, Y J Woo, H S Kim

Abstract

Androgen insensitivity syndrome[testicular feminization syndrome] is a rare inherited form of male pseudohermaphroditism that occurs in phenotypically normal women with adequate breast development, normal external genitalia, a blindedly ended vagina, absent uterus, and sparse or absent pubic and axillary hair,1 despite the normal karyotype of this condition in female, despite the normal male karyotype 46 XY.2 A case of complete testicular feminization syndrome is presented with a brief review of literatures.

Key Words: Complete testicular feminization syndrome

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