Abstract
Androgen insensitivity syndrome (AIS) is a rare disorder of sexual differentiation,
characterized by impaired responsiveness to androgens, resulting in the development
of typically female external genitalia, despite having a male chromosomal pattern
(XY). In this case report, we describe the radiological findings of two young siblings
diagnosed with AIS who presented with primary amenorrhea. The diagnosis was confirmed
on laparotomy and gonads were surgically removed in both the siblings.
Keywords
androgen insensitivity syndrome - androgens - ultrasound - magnetic resonance imaging
- primary amenorrhea - Mullerian structures - gonads - secondary sexual characteristics
