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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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Detaylı Bibliyografya
Yayımlandı:Urol Ann
Asıl Yazarlar: Gajbhiye, Vishal, Nath, Sasanka, Ghosh, Priya, Chatterjee, Argha, Haldar, Dipanjan, Das, Sukanta K.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Medknow Publications & Media Pvt Ltd 2015
Konular:
Online Erişim: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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