Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/51471
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dc.contributor.authorYitik, Ahmet Yasin-
dc.contributor.authorUfuk, Furkan-
dc.contributor.authorÇelen, Sinan-
dc.date.accessioned2023-06-13T19:19:13Z-
dc.date.available2023-06-13T19:19:13Z-
dc.date.issued2023-
dc.identifier.issn2148-9580-
dc.identifier.urihttps://doi.org/10.4274/jus.galenos.2022.2022.0015-
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/1168286-
dc.identifier.urihttps://hdl.handle.net/11499/51471-
dc.description.abstractZinner syndrome is a rare disorder, and it is associated with unilateral renal agenesis, ipsilateral ejaculatory duct atresia (obstruction), and cystic dilatation of the ipsilateral seminal vesicle. Here, we present an eighteen-year-old male with Zinner syndrome who presented to a urology clinic with perineal/pelvic pain and dysuria. We also emphasize the computed tomography and magnetic resonance imaging findings of Zinner syndrome.en_US
dc.language.isoenen_US
dc.relation.ispartofJournal of Urological Surgeryen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleA Young Boy with Renal Agenesis and Ectopic Seminal Vesicle: Zinner Syndromeen_US
dc.typeArticleen_US
dc.identifier.volume10en_US
dc.identifier.issue1en_US
dc.identifier.startpage74en_US
dc.identifier.endpage76en_US
dc.departmentPamukkale Universityen_US
dc.identifier.doi10.4274/jus.galenos.2022.2022.0015-
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.trdizinid1168286en_US
dc.institutionauthor-
item.openairetypeArticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.cerifentitytypePublications-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.01. Surgical Medicine-
Appears in Collections:Tıp Fakültesi Koleksiyonu
TR Dizin İndeksli Yayınlar Koleksiyonu / TR Dizin Indexed Publications Collection
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