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Information Journal Paper

Title

Novel Presentation of Complete Coronal Urethral Duplication: a Case Report

Pages

  4707-4712

Keywords

Abstract

 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.

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    • Cite

    APA: Copy

    Salimi, Amrollah, Rashidinia, Shervin, Eftekhari, Seyed Shahin, & Shahmoradi, sara. (2017). Novel Presentation of Complete Coronal Urethral Duplication: a Case Report. INTERNATIONAL JOURNAL OF PEDIATRICS, 5(4 (40)), 4707-4712. SID. https://sid.ir/paper/337513/en

    Vancouver: Copy

    Salimi Amrollah, Rashidinia Shervin, Eftekhari Seyed Shahin, Shahmoradi sara. Novel Presentation of Complete Coronal Urethral Duplication: a Case Report. INTERNATIONAL JOURNAL OF PEDIATRICS[Internet]. 2017;5(4 (40)):4707-4712. Available from: https://sid.ir/paper/337513/en

    IEEE: Copy

    Amrollah Salimi, Shervin Rashidinia, Seyed Shahin Eftekhari, and sara Shahmoradi, “Novel Presentation of Complete Coronal Urethral Duplication: a Case Report,” INTERNATIONAL JOURNAL OF PEDIATRICS, vol. 5, no. 4 (40), pp. 4707–4712, 2017, [Online]. Available: https://sid.ir/paper/337513/en

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