Korean J Obstet Gynecol.  1999 Jul;42(7):1599-1603.

A Case of Complete Testicular Feminization Syndrome

• Moon TS
• Rho JS
• Park JH
• Jeon DJ
• Jang YW
• Koo JN
• Park YS
• Woo YJ
• Kim HS

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.

Keyword

Complete testicular feminization syndrome

MeSH Terms

46, XY Disorders of Sex Development
Androgen-Insensitivity Syndrome*
Breast
Female
Feminization
Genitalia
Humans
Karyotype
Male
Uterus
Vagina