Complete Urethral Duplication in Children: A Case Report


Autoria(s): Roshanzamir, Fatollah; Mirshemirani, Alireza; Ghoroubi, Javad; Mahdavi, Alireza; Mohajerzadeh, Leily; Sarafi, Mehdi
Cobertura

Origin of publication: Iran

Data(s)

08/07/2016

Resumo

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.

Formato

html

Identificador

http://www.bioline.org.br/abstract?id=pe16018

Idioma(s)

en

Publicador

Tehran University of Medical Sciences Press

Relação

http://diglib.tums.ac.ir/pub/; http://www.bioline.org.br/pe

Direitos

Copyright 2016 - Iranian Journal of Pediatrics

Fonte

Iranian Journal of Pediatrics (ISSN: 1018-4406) Vol 26 Num 2

Palavras-Chave #Complete Urethral Duplication, Effman Classification, IIA1 Type, Surgical Repair
Tipo

CR