Urethral Duplication in a 7-Year-Old Boy | Journal of Paediatric Surgeons of Bangladesh

Authors

Emon Kanti MoharerAssistant Professor, Paediatric Surgery Sylhet MAG Osmani Medical College Hospital
Md Sirazul IslamAssistant Professor, Paediatric Surgery Sylhet MAG Osmani Medical College.
Kanchan Kumar DebRegistrar, Paediatric Surgery Sylhet MAG Osmani Medical College Hospital.
Tilottama Pushpita BhowmikLecturer, Pathology Sylhet MAG Osmani Medical College.

Keywords

urethra dorsal congenital double duplication

Abstract

Urethral duplication is a rare congenital anomaly, predominantly seen in males, with very few cases reported in females. This anomaly can be partial or complete and manifests with a variety of clinical symptoms including deformed penis, double urinary streams, urinary tract infections (UTIs), incontinence, urethral discharge, and outflow obstruction. This case report discusses the diagnosis, surgical management, and follow-up of a 7 years old boy with Type II A2 urethral duplication.

Journal of Paediatric Surgeons of Bangladesh (2026) Vol. 17 (1): 114–116

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Published

2026-07-09

Issue

Vol. 17 No. 1 (2026)

Section

Case Reports

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How to Cite

Moharer, E. K., Islam, M. S., Deb, K. K., & Bhowmik, T. P. (2026). Urethral Duplication in a 7-Year-Old Boy. Journal of Paediatric Surgeons of Bangladesh, 17(1), 114–116.

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