TY - JOUR ID - 8514 TI - Novel Presentation of Complete Coronal Urethral Duplication: a Case Report JO - International Journal of Pediatrics JA - IJP LA - en SN - 2345-5047 AU - Salimi, Amrollah AU - Rashidinia, Shervin AU - Eftekhari, Seyed Shahin AU - Shahmoradi, Sara AD - Department of Pediatric Surgery of Hazrat Masoume Hospital, Qom University of Medical Sciences, Qom, Iran. AD - School of Medicine, Qom University of Medical Sciences, Qom, Iran. Y1 - 2017 PY - 2017 VL - 5 IS - 4 SP - 4707 EP - 4712 KW - Appendix KW - Child KW - fistula KW - Urethra DO - 10.22038/ijp.2017.22681.1895 N2 -      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. UR - https://ijp.mums.ac.ir/article_8514.html L1 - https://ijp.mums.ac.ir/article_8514_d8ae3972d5e52fc014846d8893e3e707.pdf ER -