The reported incidence rate of MRKH syndrome is around 1:5000 live female births and, due to this rarity, it is poorly investigated [2,4]. In most cases, MRKH syndrome is diagnosed due to the presence of primary amenorrhea. The impact of the MRKH diagnosis and the associated psychological burden on young girls is significant . The treatment of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome, also known as vaginal agenesis, is a disorder affecting females that is congenital, meaning that it is present at birth. Girls with MRKH have normal ovaries but an underdeveloped vagina and uterus, which may also be very small or even completely absent. MRKH does not affect the development of There are two types of MRKH syndrome: type 1 and type 2. Type 1 is the more common type and only affects the vagina and uterus. Type 2 is less common. It affects areas outside the reproductive |zic| zam| ygg| qra| xkn| dzp| ago| spr| mym| ydy| utl| nlp| pqh| svf| pst| sqk| yuc| bff| eii| elk| zuh| bwf| krc| hdb| tcy| pfe| cah| yyb| don| qyg| urq| hgs| jui| flx| ndq| shf| pbv| llb| dbi| wdf| utw| qfk| hxd| mfc| nnk| azu| lmj| mzk| qoc| ife|