Incidental finding of Zinner syndrome in a Greek military recruit: a case report of a rare clinical entity

BACKGROUND: Zinner syndrome represents a rare congenital malformation of the urinary tract. It comprises a constellation of Wolffian duct anomalies and is almost exclusively encountered as a classic triad of seminal vesicle cysts, ejaculatory duct obstruction and renal agenesis. Patients can be eith...

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Vydáno v:Mil Med Res
Hlavní autoři: Symeonidis, Evangelos N., Gkekas, Chrysovalantis, Tsifountoudis, Ioannis, Symeonidis, Asterios, Georgiadis, Christos, Kalyvas, Vasileios, Malioris, Apostolos, Papathanasiou, Michail
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2019
Témata:
Case Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6375168/
https://ncbi.nlm.nih.gov/pubmed/30760330
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40779-019-0194-9
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