Complete Urethral Duplication in Children: A Case Report

INTRODUCTION: Urethral duplication (UD) is a rare congenital anomaly with multiple anatomical variants. CASE PRESENTATION: In this article we present a four year-old child with complete UD. The patient was admitted for hypospadias repair, in evaluation we found type IIA1 UD according to Effmann clas...

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Autores principales: Roshanzamir, Fatollah, Mirshemirani, Alireza, Ghoroubi, Javad, Mahdavi, Alireza, Mohajerzadeh, Leily, Sarafi, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906148/
https://www.ncbi.nlm.nih.gov/pubmed/27307964
http://dx.doi.org/10.5812/ijp.3620
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author Roshanzamir, Fatollah
Mirshemirani, Alireza
Ghoroubi, Javad
Mahdavi, Alireza
Mohajerzadeh, Leily
Sarafi, Mehdi
author_facet Roshanzamir, Fatollah
Mirshemirani, Alireza
Ghoroubi, Javad
Mahdavi, Alireza
Mohajerzadeh, Leily
Sarafi, Mehdi
author_sort Roshanzamir, Fatollah
collection PubMed
description INTRODUCTION: Urethral duplication (UD) is a rare congenital anomaly with multiple anatomical variants. CASE PRESENTATION: In this article we present a four year-old child with complete UD. The patient was admitted for hypospadias repair, in evaluation we found type IIA1 UD according to Effmann classification. Patient underwent hypospadias repair saving complete UD. CONCLUSIONS: After one year follow-up he has normal and continent urination.
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spelling pubmed-49061482016-06-15 Complete Urethral Duplication in Children: A Case Report Roshanzamir, Fatollah Mirshemirani, Alireza Ghoroubi, Javad Mahdavi, Alireza Mohajerzadeh, Leily Sarafi, Mehdi Iran J Pediatr Case Report INTRODUCTION: Urethral duplication (UD) is a rare congenital anomaly with multiple anatomical variants. CASE PRESENTATION: In this article we present a four year-old child with complete UD. The patient was admitted for hypospadias repair, in evaluation we found type IIA1 UD according to Effmann classification. Patient underwent hypospadias repair saving complete UD. CONCLUSIONS: After one year follow-up he has normal and continent urination. Kowsar 2016-03-05 /pmc/articles/PMC4906148/ /pubmed/27307964 http://dx.doi.org/10.5812/ijp.3620 Text en Copyright © 2016, Growth & Development Research Center http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Case Report
Roshanzamir, Fatollah
Mirshemirani, Alireza
Ghoroubi, Javad
Mahdavi, Alireza
Mohajerzadeh, Leily
Sarafi, Mehdi
Complete Urethral Duplication in Children: A Case Report
title Complete Urethral Duplication in Children: A Case Report
title_full Complete Urethral Duplication in Children: A Case Report
title_fullStr Complete Urethral Duplication in Children: A Case Report
title_full_unstemmed Complete Urethral Duplication in Children: A Case Report
title_short Complete Urethral Duplication in Children: A Case Report
title_sort complete urethral duplication in children: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906148/
https://www.ncbi.nlm.nih.gov/pubmed/27307964
http://dx.doi.org/10.5812/ijp.3620
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