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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/9121
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dc.contributor.authorChiriţa, Lilia
dc.contributor.authorBejan, Sergiu
dc.contributor.authorBobu, Victor
dc.contributor.authorGuţu, Constantin
dc.contributor.authorCaraion, Vladimir
dc.contributor.authorGaidău, M.
dc.contributor.authorPleşca, Eduard
dc.date.accessioned2020-05-06T18:15:50Z
dc.date.available2020-05-06T18:15:50Z
dc.date.issued2011
dc.identifier.citationCHIRIŢA L., BEJAN S., BOBU V., et al. Caz clinic: sindromul Mayer-Rokitansky-Kuster-Hauser, forma atipică. In: Arta Medica. 2011, nr. 2(45), pp. 154-156. ISSN 1810-1852.en_US
dc.identifier.issn1810-1852
dc.identifier.urihttp://repository.usmf.md/handle/20.500.12710/9121
dc.descriptionSecţia Urologie IMSP SCM „Sf. Treime”, Catedra Urologie şi Nefrologie Chirurgicală, USMF „N. Testemiţanu”, Al V-lea Congres de Urologie, Dializă şi Transplant Renal din Republica Moldova cu participare internaţională (1-13 iunie 2011)en_US
dc.description.abstractSummary. The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare anomaly in the prenatal development of the female genital tract. In this paper we report a clinical case of this syndrome observed in its atypical form with affected urogenital system, as well as uterine and renal agenesia. This case is interesting, as the patient did not receive any specific treatment associated with the syndrome until the age of 29. We provide a detailed description of the clinical case, its specifics and anamnesis. A literature review on the prenatal development of the female genital tract, urogenital system and the renal agenesia is also given.en_US
dc.language.isoroen_US
dc.publisherAsociaţia chirurgilor “Nicolae Anestiadi” din Republica Moldovaen_US
dc.subject.meshAbnormalities, Multiple--diagnosisen_US
dc.subject.meshUrogenital abnormalities--diagnosisen_US
dc.subject.meshUterus--abnormalitiesen_US
dc.subject.meshVagina--abnormalitiesen_US
dc.subject.meshOvary--abnormalitiesen_US
dc.subject.meshKidney--abnormalitiesen_US
dc.subject.meshCase Reportsen_US
dc.titleCaz clinic: sindromul Mayer-Rokitansky-Kuster-Hauser, forma atipicăro
dc.title.alternativeClinical case: Mayer-Rokitansky-Kuster-Hauser syndrome, atypic formen_US
dc.typeArticleen_US
Appears in Collections:Arta Medica Vol. 45 No.2, 2011 ediţie specială

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