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dc.contributor.authorSelvi, İsmail
dc.contributor.authorEkmekcioglu, Oguz
dc.contributor.authorAKINSAL, EMRE CAN
dc.contributor.authorGolbasi, Abdullah
dc.contributor.authorİMAMOĞLU, HAKAN
dc.contributor.authorBaydilli, Numan
dc.date.accessioned2021-12-10T11:43:34Z
dc.date.available2021-12-10T11:43:34Z
dc.identifier.citationBaydilli N., AKINSAL E. C. , Selvi İ., Golbasi A., İMAMOĞLU H., Ekmekcioglu O., "A Rare Case of Partial Unilateral Corpus Cavernosum Agenesis With Concomitant Multiple Genitourinary Anomalies", UROLOGY, cilt.143, ss.234-237, 2020
dc.identifier.issn0090-4295
dc.identifier.othervv_1032021
dc.identifier.otherav_909e3f35-0637-430c-acf6-c5536b5baf65
dc.identifier.urihttp://hdl.handle.net/20.500.12627/172495
dc.identifier.urihttps://doi.org/10.1016/j.urology.2020.05.008
dc.description.abstractCongenital penile agenesis is a rare condition with an incidence of 1 in 30 million, while other congenital malformations of the cavernous bodies are much less common. In a few cases in the literature, it has been reported that the reason for consulting a physician with these conditions is the insufficient erection. As a first reported case, we present a 16-year-old male patient with partial unilateral corpus cavernosum agenesis accompanying genitourinary anomalies. (c) 2020 Elsevier Inc.
dc.language.isoeng
dc.subjectNefroloji
dc.subjectNephrology
dc.subjectUrology
dc.subjectHealth Sciences
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectÜROLOJİ VE NEFROLOJİ
dc.titleA Rare Case of Partial Unilateral Corpus Cavernosum Agenesis With Concomitant Multiple Genitourinary Anomalies
dc.typeMakale
dc.relation.journalUROLOGY
dc.contributor.department, ,
dc.identifier.volume143
dc.identifier.startpage234
dc.identifier.endpage237
dc.contributor.firstauthorID2696654


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