Caz clinic: sindromul Mayer-Rokitansky-Kuster-Hauser, forma atipică

Abstract

Summary. The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare anomaly in the prenatal development of the female genital tract. In this paper we report a clinical case of this syndrome observed in its atypical form with affected urogenital system, as well as uterine and renal agenesia. This case is interesting, as the patient did not receive any specific treatment associated with the syndrome until the age of 29. We provide a detailed description of the clinical case, its specifics and anamnesis. A literature review on the prenatal development of the female genital tract, urogenital system and the renal agenesia is also given.