Question 187 · LEK · Congenital malformations of the female genital organs

A feature common for the Mayer-Rokitansky-Kustner-Hauser syndrome and complete androgen insensitivity syndrome is:

  1. A. XY karyotype.
  2. B. XX karyotype.
  3. C. lack of the uterus and vagina.
  4. D. defect of the androgen receptor gene.
  5. E. presence of testicles in the abdominal cavity.
Hint

One condition is 46,XX Müllerian agenesis, the other a 46,XY androgen receptor defect; what anatomical finding do they share?

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