Korean J Obstet Gynecol.  2003 Jan;46(1):166-170.

A case of complete testicular feminization syndrome with Inguinal Hernias

Affiliations
  • 1Department of Obstetrics and Gynecology, National Medical Center, Seoul, Korea.

Abstract

Complete testicular feminization syndrome (androgen insensitivity syndrome) is the most common form of male pseudohermaphroditism, transmitted by means of maternal X-linked recessive gene. This syndrome is marked by unique combination; Normal female phenotype, normal male karyotype, 46,XY, normal or slightly elevated male blood testosterone levels and a high LH. Clinically, the diagnosis should be considered in a female with inguinal hernias, a patient with primary amenorrhea and absent uterus. we present a case testicular feminization syndrome with blindly ended vagina and inguinal masses with a brief review of literatures.

Keyword

Testicular feminization syndrome

MeSH Terms

46, XY Disorders of Sex Development
Amenorrhea
Androgen-Insensitivity Syndrome*
Diagnosis
Female
Genes, Recessive
Hernia, Inguinal*
Humans
Karyotype
Male
Phenotype
Testosterone
Uterus
Vagina
Testosterone
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