Mayerrokitanskykusterhauser syndrome, sometimes simply called rokitansky syndrome or vaginal aplasia of the uterus, is a congenital condition present at birth that is characterized by the absence of the uterus and vagina, and ovaries are present and also the external genitalia are normal. Rbcp vaginal reconstruction by neurovascular pudendal thigh. The features, in addition to congenital absence of the vagina, are normal female secondary sexual characteristics, rudimentary uterus in the form of bilateral and noncanaliculated muscular buds, normal tubes and ovaries and normal endocrine and cytogenetic evaluations. Omim entry % 277000 mayerrokitanskykusterhauser syndrome. Mayerrokitanskykusterhauser syndrome mrkh is characterized by uterovaginal atresia in an otherwise phenotypically normal female with a normal 46,xx karyotype. Suas caracteristicas sao ausencia total ou parcial da vagina, anomalias uterinas e tubarias. Mayerrokitanskykuester syndrome a congenital defect characterized by impaired differentiation of mullerian duct. Sumario revista espanola endocrinologia pediatrica. Malattie rare, sul portale tu e duchenne tutte le risposte.
Roki news sindrome di mayer rokitansky kuster hauser. Rbcp vaginal reconstruction by neurovascular pudendal. Rokitansky syndrome definition of rokitansky syndrome by. Mayer rokitansky kusterhauser syndrome, sometimes simply called rokitansky syndrome or vaginal aplasia of the uterus, is a congenital condition present at birth that is characterized by the absence of the uterus and vagina, and ovaries are present and also the external genitalia are normal. Sindrome di mayer rokitansky kuster hauser, ecco di cosa.
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