Novel Presentation of Complete Coronal Urethral Duplication: a Case Report

Salimi, Amrollah and Rashidinia, Shervin and Eftekhari, Seyed Shahin and Shahmoradi, Sara (2017) Novel Presentation of Complete Coronal Urethral Duplication: a Case Report. International Journal of Pediatrics, 5 (4). pp. 4707-4712.

IJP_Volume 5_Issue 4_Pages 4707-4712.pdf

Download (488kB) | Preview
Official URL:


Urethralduplication is a rare condition occurs as a congenital malformation either independently or in the setting of other congenital malformations such as caudal duplication syndrome. Its prevalence becomes even rarer if it manifests as two side-by-side tracts in coronal plan.Nonetheless, we introduce a unique presentation of complete coronal urethral duplication accompanied by astounding manifestations of gastrointestinal malformations different from what is expected for a normal hind gut or caudal duplication syndrome. A 6-year-old boy with complete coronal duplication of urethra along with duplication of appendix, sigmoid and rectum as well as developmental delay, attracted our attention to report.

Item Type: Article
Subjects: WA Public Health
WS Pediatrics
Divisions: Journals > International J Pediatrics
Depositing User: IJP IJP
Date Deposited: 23 Sep 2017 23:39
Last Modified: 23 Sep 2017 23:39

Actions (login required)

View Item View Item