A Rare Presentation of Urethral Duplication in Conjunction With Anorectal Malformation Observed in a Male Infant

A Rare Presentation of Urethral Duplication in Conjunction With Anorectal Malformation Observed in a Male Infant

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Anorectal malformation (ARM) refers to a group of Womens L/S Onepiece Suit congenital anomalies that affect the anus, rectum, and sometimes the urinary and reproductive tracts.A full-term male newborn was diagnosed with ARM and rectoperineal (scrotal) fistula during a first clinical screening examination at birth.He also had urethral duplication on the micturating cystourethrogram (MCUG) scan performed on Day 2 of life.

The child underwent transverse colostomy at 24 h of life and corrective surgery (posterior sagittal anorectoplasty and urethroplasty) at 6 months of life, followed by colostomy closure after 3 months.This case highlights the importance of the first newborn clinical screening examination to rule out major congenital malformation and the thorough evaluation for associated urogenital defects NEFF KI7862FF0G Integrated 60/40 Frost Free Fridge Freezer in the case of ARM before definitive corrective surgeries for better clinical outcomes.