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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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Dades bibliogràfiques
Publicat a:Urol Ann
Autors principals: Gajbhiye, Vishal, Nath, Sasanka, Ghosh, Priya, Chatterjee, Argha, Haldar, Dipanjan, Das, Sukanta K.
Format: Artigo
Idioma:Inglês
Publicat: Medknow Publications & Media Pvt Ltd 2015
Matèries:
Accés en línia: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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