Androgen insensitivity syndrome (testicular feminization)
Androgen insensitivity (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 vagina of variable depth, absent uterus, and sparse or absent pubic hair and axillary hair.

These patients have male karyotype (XY) and negative sex chromatin. The gonad (undescended testis) may be intraabdominal, inguinal, or labial.

In the present case, published in The Journal of Obstetrics and Gynecology of India, chromosome study has been carried out and 46, XY karyotype has been detected in the phenotypic female.

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