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CASE REPORT
Year : 2015  |  Volume : 7  |  Issue : 1  |  Page : 91-93

Complete duplication of the urinary bladder: An extremely rare congenital anomaly


1 Department of Paediatric Surgery, Medical College and Hospital, The west Bengal University of Health Sciences, Kolkata, West Bengal, India
2 Department of Radiodiagnosis, Medical College and Hospital, The west Bengal University of Health Sciences, Kolkata, West Bengal, India

Correspondence Address:
Vishal Gajbhiye
21 f/3, P.B.C. Road, Near Swiss Park Nursing Home, Kolkata Pin - 700033
India
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DOI: 10.4103/0974-7796.148629

PMID: 25657554

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A case of complete bladder duplication with urethra duplication, diphallus, anorectal malformation and rightsided renal agensis with ipsilateral gonadal agenesisis was reported because of its rarity. Possible deranged embryology resulting in these anomalies has been reviewed with relevant hypothesis. The patient underwent several investigations and undergoing multistage surgical intervention.


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