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

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...

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書目詳細資料
發表在:Urol Ann
Main Authors: Gajbhiye, Vishal, Nath, Sasanka, Ghosh, Priya, Chatterjee, Argha, Haldar, Dipanjan, Das, Sukanta K.
格式: Artigo
語言:Inglês
出版: Medknow Publications & Media Pvt Ltd 2015
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC4310128/
https://ncbi.nlm.nih.gov/pubmed/25657554
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0974-7796.148629
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