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A case of complete testicular feminization syndrome with Inguinal Hernias / 대한산부인과학회잡지
Korean Journal of Obstetrics and Gynecology ; : 166-170, 2003.
Article in Korean | WPRIM | ID: wpr-186670
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.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Phenotype / Androgen-Insensitivity Syndrome / Testosterone / Uterus / Vagina / Diagnosis / Disorder of Sex Development, 46,XY / Karyotype / Amenorrhea / Genes, Recessive Type of study: Diagnostic study Limits: Female / Humans / Male Language: Korean Journal: Korean Journal of Obstetrics and Gynecology Year: 2003 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Phenotype / Androgen-Insensitivity Syndrome / Testosterone / Uterus / Vagina / Diagnosis / Disorder of Sex Development, 46,XY / Karyotype / Amenorrhea / Genes, Recessive Type of study: Diagnostic study Limits: Female / Humans / Male Language: Korean Journal: Korean Journal of Obstetrics and Gynecology Year: 2003 Type: Article