Mayer-Rokitansky-Kuster-Hauser syndrome type II: A rare case.

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dc.contributor.authorPai, Anand
dc.contributor.authorShakir, Mohammad
dc.date.accessioned2013-08-01T09:32:25Z
dc.date.available2013-08-01T09:32:25Z
dc.date.issued2013-01
dc.description.abstractMayer-Rokitansky-Kuster-Hauser (MRKH) is a malformation complex comprising absent vagina and absent or rudimentary uterus. MRKH syndrome may be attributed to an initial affection of the intermediate mesoderm consequently leading (by the end of the 4th week of fetal life) to an alteration of the blastema of the cervicothoracicsomites and the pronephricducts. These latter subsequently induce the differentiation of the mesonephric and then the Wolffian and Mullerian ducts. There are very sparse such cases reported. We present a case of type II MRKH or Mullerian renal cervical somite association (i.e., Mullerian duct aplasia, renal dysplasia, and cervical somite anomalies).en_US
dc.identifier.citationPai Anand, Shakir Mohammad. Mayer-Rokitansky-Kuster-Hauser syndrome type II: A rare case. Indian Journal of Human Genetics. 2013 Jan; 19(1): 113-115.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/147650
dc.language.isoenen_US
dc.source.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3722622/?report=classicen_US
dc.subjectDandy Walker malformationen_US
dc.subjectmayer-rokitansky-kuster-hauser syndrome type IIen_US
dc.subjectmullerian agenesisen_US
dc.subjectrenal agenesisen_US
dc.subject.mesh46, XX Disorders of Sex Development --epidemiology
dc.subject.meshAbnormalities, Multiple
dc.subject.meshAdult
dc.subject.meshCongenital Abnormalities
dc.subject.meshDandy-Walker Syndrome --epidemiology
dc.subject.meshDandy-Walker Syndrome --genetics
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshKidney --abnormalities
dc.subject.meshKidney Diseases --congenital
dc.subject.meshMullerian Ducts --abnormalities
dc.titleMayer-Rokitansky-Kuster-Hauser syndrome type II: A rare case.en_US
dc.typeArticleen_US
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