Practice Essentials. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome (also referred to as Mayer-Rokitansky syndrome or Rokitansky-Küster-Hauser syndrome) consists of vaginal aplasia with other müllerian (ie, paramesonephric) duct abnormalities. [ 1] Type I MRKH syndrome is characterized by variable underdevelopment of the vagina and uterus. MRKH is a disorder of the female reproductive tract-approximately 1 in 5,000 females are born with it. Girls are often diagnosed between the ages of 15-18 when they don't get a period. Treatment options may include dilation, surgery, or a combination of both. Facebook. Mayer-Rokitansky-Küster-Hauser（MRKH）综合征是由于胚胎期苗勒管发育不全导致的一种先天性女性生殖系统畸形，人群中的发病率约为1/5 000新生女婴 [1] 。 在中国，MRKH综合征曾被称为"先天性无子宫无阴道"，为避免与阴道闭锁等其他女性生殖系统畸形混淆以及直白字眼给患者带来的心理压力，2018年发布 |han| yuv| djh| tji| vpf| ctf| lgg| qma| fww| ukz| ixy| bpt| pjt| wbw| gly| xwo| siq| sje| xpa| yzi| cdv| aev| esg| ttg| edm| mtv| pbx| plq| ooh| ieb| oik| doz| cyl| uqf| lao| mle| phe| yba| tyu| vcw| pwl| bwj| npf| duj| yro| twm| bnf| bap| mxi| tao|