Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/1993
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dc.contributor.authorSalbacak, Ahmet-
dc.contributor.authorTezer, Murat-
dc.date.accessioned2022-08-16T11:42:58Z-
dc.date.available2022-08-16T11:42:58Z-
dc.date.issued2017-
dc.identifier.urihttp://doi.org/10.1016/j.jasi.2017.10.004-
dc.identifier.urihttp://earsiv.odu.edu.tr:8080/xmlui/handle/11489/1993-
dc.description.abstractDuplication of the vas deferens is a rare congenital anomaly, and it can be complete or partial. It is usually discovered as an incidental finding during elective operations stich as a vasectomy, herniorrhaphy or varicocelectomy. During the educational dissection of a 72-year-old cadaver, a complete vas deferens duplication was observed on the left. If a vas deferens duplication is not appropriately diagnosed, it can result in surgical complications or an unsuccessful vasectomy. Screening for renal agenesis should be performed in patients with duplication of the vas deferens. (C) 2017 Anatomical Society of India. Published by Elsevier, a division of RELX India, Pvt. Ltd. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherELSEVIER SCIENCE BV, PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDSen_US
dc.relation.isversionof10.1016/j.jasi.2017.10.004en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBILATERAL DUPLICATION; TRUE DUPLICATION; EPIDIDYMISen_US
dc.subjectCongenital abnormalities; Duplication; Vas deferensen_US
dc.titleUnilateral complet duplication of the vas deferens: Cadaveric case reporten_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF THE ANATOMICAL SOCIETY OF INDIAen_US
dc.contributor.departmentOrdu Üniversitesien_US
dc.contributor.authorID0000-0003-1790-5204en_US
dc.identifier.volume66en_US
dc.identifier.startpageS13en_US
dc.identifier.endpageS16en_US
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