Uethralduplication is very rare congenitalanomaly with ill defined etiology. Veryfew cases have beenreported in literature till date. Patients may presentwith urinary incontinence, abnormal or dual urinary stream, recurrent urinarytract infections and sometimes associated penile deformity. Aim of presentingthis case report is to limelight one of such rare presentations. Herewith reporting acase of 16 months old baby boy presented with history of recurrent urinary tract infection, solitary kidney with grade 4 primary vesico-ureteric reflux and duplication of urethra. Diagnosis and treatment plan in such cases require a multistage approach.
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