Novel Presentation of Complete Coronal Urethral Duplication: a Case Report
محل انتشار: مجله بین المللی کودکان، دوره: 5، شماره: 4
سال انتشار: 1396
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 409
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شناسه ملی سند علمی:
JR_INJPM-5-4_007
تاریخ نمایه سازی: 20 مهر 1398
چکیده مقاله:
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.
نویسندگان
Amrollah Salimi
Department of Pediatric Surgery of Hazrat Masoume Hospital, Qom University of Medical Sciences, Qom, Iran.
Shervin Rashidinia
School of Medicine, Qom University of Medical Sciences, Qom, Iran.
Seyed Shahin Eftekhari
School of Medicine, Qom University of Medical Sciences, Qom, Iran.
Sara Shahmoradi
School of Medicine, Qom University of Medical Sciences, Qom, Iran.