Clinical case of prenatal diagnosis of testicular feminization syndrome

A case of prenatal ultrasound diagnosis of testicular feminization syndrome (Morris syndrome) is described. At the stage of pregnancy, when determining the sex of the fetus by a non-invasive prenatal test, the male genetic sex was revealed. A transabdominal examination in the third trimester of pregnancy revealed female-type external genitalia and a lack of visualization of the uterus. The diagnosis was confirmed after birth, upon examination - the external genitalia are developed according to the female type, the karyotype of the child is male (46,XY). When clarifying the medical history, the presence of Morris syndrome in the patient's own sister.