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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Detalles Bibliográficos
Autores principales: Gajbhiye, Vishal, Nath, Sasanka, Ghosh, Priya, Chatterjee, Argha, Haldar, Dipanjan, Das, Sukanta K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310128/
https://www.ncbi.nlm.nih.gov/pubmed/25657554
http://dx.doi.org/10.4103/0974-7796.148629

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310128/
https://www.ncbi.nlm.nih.gov/pubmed/25657554
http://dx.doi.org/10.4103/0974-7796.148629

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