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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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| 出版年: | Urol Ann |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Medknow Publications & Media Pvt Ltd
2015
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| 主題: | |
| オンライン･アクセス: | 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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