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Two brothers with congenital bulbar urethral stricture: case report of a very rare condition

Congenital urethral stricture is rare. It has been reported in only four sets of brothers. We report the fifth set of brothers. Cases of two brothers aged 23 and 18 years old diagnosed with low urinary tract symptoms are presented. We diagnosed an apparently congenital urethral stricture in both bro...

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Autores principales: Mokadem, Seif, Saadi, Ahmed, Hermi, Amine, Boussaffa, Hamza, Chakroun, Marouene, Ben Slama, Mohamed Riadh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9970558/
https://www.ncbi.nlm.nih.gov/pubmed/36860355
http://dx.doi.org/10.1093/jscr/rjad072
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author Mokadem, Seif
Saadi, Ahmed
Hermi, Amine
Boussaffa, Hamza
Chakroun, Marouene
Ben Slama, Mohamed Riadh
author_facet Mokadem, Seif
Saadi, Ahmed
Hermi, Amine
Boussaffa, Hamza
Chakroun, Marouene
Ben Slama, Mohamed Riadh
author_sort Mokadem, Seif
collection PubMed
description Congenital urethral stricture is rare. It has been reported in only four sets of brothers. We report the fifth set of brothers. Cases of two brothers aged 23 and 18 years old diagnosed with low urinary tract symptoms are presented. We diagnosed an apparently congenital urethral stricture in both brothers. Internal urethrotomy was performed in both cases. Both are asymptomatic after 24 and 20 months of follow-up. Congenital urethral strictures are probably more frequent than we think. We suggest that a congenital origin should be considered if there is no history of infections or trauma.
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spelling pubmed-99705582023-02-28 Two brothers with congenital bulbar urethral stricture: case report of a very rare condition Mokadem, Seif Saadi, Ahmed Hermi, Amine Boussaffa, Hamza Chakroun, Marouene Ben Slama, Mohamed Riadh J Surg Case Rep Case Report Congenital urethral stricture is rare. It has been reported in only four sets of brothers. We report the fifth set of brothers. Cases of two brothers aged 23 and 18 years old diagnosed with low urinary tract symptoms are presented. We diagnosed an apparently congenital urethral stricture in both brothers. Internal urethrotomy was performed in both cases. Both are asymptomatic after 24 and 20 months of follow-up. Congenital urethral strictures are probably more frequent than we think. We suggest that a congenital origin should be considered if there is no history of infections or trauma. Oxford University Press 2023-02-27 /pmc/articles/PMC9970558/ /pubmed/36860355 http://dx.doi.org/10.1093/jscr/rjad072 Text en Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2023. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Mokadem, Seif
Saadi, Ahmed
Hermi, Amine
Boussaffa, Hamza
Chakroun, Marouene
Ben Slama, Mohamed Riadh
Two brothers with congenital bulbar urethral stricture: case report of a very rare condition
title Two brothers with congenital bulbar urethral stricture: case report of a very rare condition
title_full Two brothers with congenital bulbar urethral stricture: case report of a very rare condition
title_fullStr Two brothers with congenital bulbar urethral stricture: case report of a very rare condition
title_full_unstemmed Two brothers with congenital bulbar urethral stricture: case report of a very rare condition
title_short Two brothers with congenital bulbar urethral stricture: case report of a very rare condition
title_sort two brothers with congenital bulbar urethral stricture: case report of a very rare condition
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9970558/
https://www.ncbi.nlm.nih.gov/pubmed/36860355
http://dx.doi.org/10.1093/jscr/rjad072
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