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Female Urethral Duplication: Rare Anomaly with Unusual Presentation
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نویسنده
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Solanki Shailesh ,Babu M. Narendra ,Jadhav Vinay ,Gowrishankar ,Ramesh S.
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منبع
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journal of surgical technique and case report - 2015 - دوره : 7 - شماره : 1 - صفحه:1 -3
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چکیده
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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.
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کلیدواژه
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Ambiguous genitalia ,female pseudohermaphroditism ,urethral duplication
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آدرس
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Indira Gandhi Institute of Child Health Hospital, Department of Pediatric Surgery, India, Indira Gandhi Institute of Child Health Hospital, Department of Pediatric Surgery, India, Indira Gandhi Institute of Child Health Hospital, Department of Pediatric Surgery, India, Indira Gandhi Institute of Child Health Hospital, Department of Pediatric Surgery, India, Indira Gandhi Institute of Child Health Hospital, Department of Pediatric Surgery, India
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Authors
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Gowrishankar
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