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The remnant of a congenital, blind- ended megaureter in a 23-year-old woman causing chronic pain and urinary infections

Multicystic dysplastic kidney (MCDK) is a congenital anomaly as the result of abnormal interaction between the ureteric bud and metanephric mesenchyme. Unilateral MCDK can be associated with other anomalies of the genitourinary tract. Relatively rare associated anomaly is the presence of ipsilateral...

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Detalles Bibliográficos
Main Authors: Pejcic, Tomislav, Markovic, Biljana, Dzamic, Zoran, Radovanovic, Milan, Hadzi-Djokic, Jovan
Formato: Artigo
Idioma:Inglês
Publicado: Polish Urological Association 2013
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3974469/
https://ncbi.nlm.nih.gov/pubmed/24707381
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5173/ceju.2013.03.art25
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