| dc.contributor.author |
Salbacak, Ahmet |
|
| dc.contributor.author |
Tezer, Murat |
|
| dc.date.accessioned |
2022-08-16T11:42:58Z |
|
| dc.date.available |
2022-08-16T11:42:58Z |
|
| dc.date.issued |
2017 |
|
| dc.identifier.uri |
http://doi.org/10.1016/j.jasi.2017.10.004 |
|
| dc.identifier.uri |
http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/1993 |
|
| dc.description.abstract |
Duplication 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.iso |
eng |
en_US |
| dc.publisher |
ELSEVIER SCIENCE BV, PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS |
en_US |
| dc.relation.isversionof |
10.1016/j.jasi.2017.10.004 |
en_US |
| dc.rights |
info:eu-repo/semantics/closedAccess |
en_US |
| dc.subject |
BILATERAL DUPLICATION; TRUE DUPLICATION; EPIDIDYMIS |
en_US |
| dc.subject |
Congenital abnormalities; Duplication; Vas deferens |
en_US |
| dc.title |
Unilateral complet duplication of the vas deferens: Cadaveric case report |
en_US |
| dc.type |
article |
en_US |
| dc.relation.journal |
JOURNAL OF THE ANATOMICAL SOCIETY OF INDIA |
en_US |
| dc.contributor.department |
Ordu Üniversitesi |
en_US |
| dc.contributor.authorID |
0000-0003-1790-5204 |
en_US |
| dc.identifier.volume |
66 |
en_US |
| dc.identifier.startpage |
S13 |
en_US |
| dc.identifier.endpage |
S16 |
en_US |