dc.contributor.author | Selvi, İsmail | |
dc.contributor.author | Ekmekcioglu, Oguz | |
dc.contributor.author | AKINSAL, EMRE CAN | |
dc.contributor.author | Golbasi, Abdullah | |
dc.contributor.author | İMAMOĞLU, HAKAN | |
dc.contributor.author | Baydilli, Numan | |
dc.date.accessioned | 2021-12-10T11:43:34Z | |
dc.date.available | 2021-12-10T11:43:34Z | |
dc.identifier.citation | Baydilli 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.issn | 0090-4295 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_909e3f35-0637-430c-acf6-c5536b5baf65 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/172495 | |
dc.identifier.uri | https://doi.org/10.1016/j.urology.2020.05.008 | |
dc.description.abstract | Congenital 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.iso | eng | |
dc.subject | Nefroloji | |
dc.subject | Nephrology | |
dc.subject | Urology | |
dc.subject | Health Sciences | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | İç Hastalıkları | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Klinik Tıp | |
dc.subject | ÜROLOJİ VE NEFROLOJİ | |
dc.title | A Rare Case of Partial Unilateral Corpus Cavernosum Agenesis With Concomitant Multiple Genitourinary Anomalies | |
dc.type | Makale | |
dc.relation.journal | UROLOGY | |
dc.contributor.department | , , | |
dc.identifier.volume | 143 | |
dc.identifier.startpage | 234 | |
dc.identifier.endpage | 237 | |
dc.contributor.firstauthorID | 2696654 | |