Complete Urethral Duplication in Children: A Case Report

نویسندگان

  • Fatollah Roshanzamir
  • Alireza Mirshemirani
  • Javad Ghoroubi
  • Alireza Mahdavi
  • Leily Mohajerzadeh
  • Mehdi Sarafi
چکیده

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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عنوان ژورنال:

دوره 26  شماره 

صفحات  -

تاریخ انتشار 2016