Title of article
Female Urethral Duplication: Rare Anomaly with Unusual Presentation
Author/Authors
Solanki, Shailesh Indira Gandhi Institute of Child Health Hospital - Department of Pediatric Surgery, India , Babu, M. Narendra Indira Gandhi Institute of Child Health Hospital - Department of Pediatric Surgery, India , Jadhav, Vinay Indira Gandhi Institute of Child Health Hospital - Department of Pediatric Surgery, India , Gowrishankar Indira Gandhi Institute of Child Health Hospital - Department of Pediatric Surgery, India , Ramesh, S. Indira Gandhi Institute of Child Health Hospital - Department of Pediatric Surgery, India
From page
1
To page
3
Abstract
Urethral duplication (UD) in females is a rare congenital anomaly and requires a high degree of clinical suspicion for diagnosis. The preoperative evaluation requires thorough investigations to delineate anatomy which is imperative for surgical reconstruction to provide excellent functional and cosmetic outcome. We describe the successful management of a 6-year-old girl with UD (presented as ambiguous genitalia and urinary incontinence) along with a review of pertinent literature.
Keywords
Ambiguous genitalia , female pseudohermaphroditism , urethral duplication
Journal title
Journal of Surgical Technique and Case Report
Journal title
Journal of Surgical Technique and Case Report
Record number
2579143
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