СИНДРОМ ПОЛИКИСТОЗНЫХ ЯИЧНИКОВ ПРИ АПЛАЗИИ ВЛАГАЛИЩА И МАТКИ

Аннотация

Kin and uterine aplasia (Mayer-Rokitansky-Kuster-Hauser syndrome MRSS) aellar ginsy can be considered a congenital disease characterized by a dysmorphic genesis of ginsy AZO, divided into a normal karyotype (46 XX) of cholera by the nature of the violation of the rivo-zhlanma of the yollars of Muller, divided by nodal recursion of the aellar ginsy of the yollars [12]. Anomaly of reproduction of the gastrointestinal tract AZO, exogen, endothelial tasir in accordance with the effects of ferromesonephral (Muller) excision of the caudal part of the gallbladder, elongation of organs, relapse of organs, anomalies of the development of the siydik azhratish system in 40% of cases (agenesis of the buirak in one direction), intestines (intestinal atresia of the Orca), bones (buttock atresia) scoliosis) and in combination with cardiac nuances [ 3.6]. Aellar ginsey azolar relapse relapse occurs in 3-4% of cases, is characterized by a violation of the reproductive system in 6,7-25% of cases. Ginsi azolar reported anomalies in current vacts increased by 14%, environmental emanation of the case