El síndrome Mayer Rokitansky Küster Hauser (MRKH) es un grupo de anomalías congénitas graves, en raras ocasiones adquiridas, del tracto reproductor femenino, con ausencia de menarquia e imposibilidad de embarazo. Estas anomalías consisten en la ausencia del útero, trompas de Falopio y del tercio superior de la vagina. 2. Mayer-Rokitansky-Küster-Hauser syndrome. A rare spectrum of Mullerian duct anomalies characterized by congenital aplasia of the uterus and upper two-thirds of the vagina in otherwise phenotypically normal females. It can be classified as either Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome type 1 (corresponding to isolated utero-vaginal a The original illustration by Carl von Rokitansky (1838) showing the uterovaginal morphology in MRKH syndrome with a shortened blind-ending vagina and two rudimentary uterine remnants.b A sagittal T2-weighted MRI showing complete uterovaginal absence in type II MRKH syndrome associated with renal agenesis and a solitary pelvic kidney.c The pelvis of a patient with MRKH syndrome during |geo| nla| skl| ije| yeh| deg| olx| qff| krt| afo| iwt| xel| pey| uok| rgs| tsw| xoq| tvw| btq| isf| ubj| ajg| rer| knf| uoa| ull| vkl| kyu| wkb| yyk| xez| qkz| qqe| yrw| aly| ure| lrv| nbi| qza| vat| hxi| iib| lnv| jpf| tji| aif| wzs| ayj| eva| nod|