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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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| Publicado no: | Urol Ann |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2015
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| Assuntos: | |
| Acesso em linha: | 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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