@article { author = {Salimi, Amrollah and Rashidinia, Shervin and Eftekhari, Seyed Shahin and Shahmoradi, Sara}, title = {Novel Presentation of Complete Coronal Urethral Duplication: a Case Report}, journal = {International Journal of Pediatrics}, volume = {5}, number = {4}, pages = {4707-4712}, year = {2017}, publisher = {Mashhad University of Medical Sciences}, issn = {2345-5047}, eissn = {2345-5055}, doi = {10.22038/ijp.2017.22681.1895}, abstract = {     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.}, keywords = {Appendix,Child,fistula,Urethra}, url = {https://ijp.mums.ac.ir/article_8514.html}, eprint = {https://ijp.mums.ac.ir/article_8514_d8ae3972d5e52fc014846d8893e3e707.pdf} }