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Paper Information

Journal:   INTERNATIONAL JOURNAL OF PEDIATRICS   april 2017 , Volume 5 , Number 4 (40); Page(s) 4707 To 4712.

Novel Presentation of Complete Coronal Urethral Duplication: a Case Report

Author(s):  Salimi Amrollah, Rashidinia Shervin, Eftekhari Seyed Shahin, Shahmoradi sara*
* School of Medicine, Qom University of Medical Sciences, Qom, Iran
Urethral duplication 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.
Keyword(s): Appendix,Child,Fistula,Urethra
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