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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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Библиографические подробности
Опубликовано в: :Urol Ann
Главные авторы: Gajbhiye, Vishal, Nath, Sasanka, Ghosh, Priya, Chatterjee, Argha, Haldar, Dipanjan, Das, Sukanta K.
Формат: Artigo
Язык:Inglês
Опубликовано: Medknow Publications & Media Pvt Ltd 2015
Предметы:
Online-ссылка: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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