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Glandular diphallus with urethral duplication: Conventional technique for a rare congenital anomaly
Diphallus is a rare anomaly and its association with urethral duplication is extremely rare. Numerous associated genitourinary and gastrointestinal anomalies have been reported with this condition. Challenges in the management are incorporation of the glans and the dominant urethra during reconstruc...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626927/ https://www.ncbi.nlm.nih.gov/pubmed/26604454 http://dx.doi.org/10.4103/0970-1591.166458 |
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author | Aihole, Jayalaxmi S. Babu, Narendra Shankar, Gauri |
author_facet | Aihole, Jayalaxmi S. Babu, Narendra Shankar, Gauri |
author_sort | Aihole, Jayalaxmi S. |
collection | PubMed |
description | Diphallus is a rare anomaly and its association with urethral duplication is extremely rare. Numerous associated genitourinary and gastrointestinal anomalies have been reported with this condition. Challenges in the management are incorporation of the glans and the dominant urethra during reconstruction. We report the successful management of a case of glandular diphallus with complete urethral duplication retaining the dorsal urethra. |
format | Online Article Text |
id | pubmed-4626927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-46269272015-11-24 Glandular diphallus with urethral duplication: Conventional technique for a rare congenital anomaly Aihole, Jayalaxmi S. Babu, Narendra Shankar, Gauri Indian J Urol Case Report Diphallus is a rare anomaly and its association with urethral duplication is extremely rare. Numerous associated genitourinary and gastrointestinal anomalies have been reported with this condition. Challenges in the management are incorporation of the glans and the dominant urethra during reconstruction. We report the successful management of a case of glandular diphallus with complete urethral duplication retaining the dorsal urethra. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4626927/ /pubmed/26604454 http://dx.doi.org/10.4103/0970-1591.166458 Text en Copyright: © Indian Journal of Urology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution NonCommercial ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Aihole, Jayalaxmi S. Babu, Narendra Shankar, Gauri Glandular diphallus with urethral duplication: Conventional technique for a rare congenital anomaly |
title | Glandular diphallus with urethral duplication: Conventional technique for a rare congenital anomaly |
title_full | Glandular diphallus with urethral duplication: Conventional technique for a rare congenital anomaly |
title_fullStr | Glandular diphallus with urethral duplication: Conventional technique for a rare congenital anomaly |
title_full_unstemmed | Glandular diphallus with urethral duplication: Conventional technique for a rare congenital anomaly |
title_short | Glandular diphallus with urethral duplication: Conventional technique for a rare congenital anomaly |
title_sort | glandular diphallus with urethral duplication: conventional technique for a rare congenital anomaly |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626927/ https://www.ncbi.nlm.nih.gov/pubmed/26604454 http://dx.doi.org/10.4103/0970-1591.166458 |
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