Ischiopagus Which is the Rarest Form of Heteropagus Along With Ambiguous Genitalia and Kidney Agenesis: A Case Report
dc.authorid | Bertan Akar / 0000-0003-0494-6867 | |
dc.authorid | Emin Haqverdiyev / 0000-0001-7562-9696 | |
dc.authorid | Reyhan Aslancan / 0000-0001-5092-3151 | |
dc.authorid | Gokhan Gümüştaş / 0000-0003-3364-8893 | |
dc.authorid | Eray Çalışkan / 0000-0002-6799-5909 | |
dc.authorwosid | Bertan Akar / CCD-2869-2022 | |
dc.contributor.author | Akar, Bertan | |
dc.contributor.author | Haqverdiyev, Emin | |
dc.contributor.author | Aslancan, Reyhan | |
dc.contributor.author | Gümüştaş, Gokhan | |
dc.contributor.author | Çalışkan, Eray | |
dc.date.accessioned | 2025-04-18T09:17:52Z | |
dc.date.available | 2025-04-18T09:17:52Z | |
dc.date.issued | 2020 | |
dc.department | İstinye Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü | |
dc.description.abstract | Parasitic twin (heteropagus) is a term to describe an incomplete fetus which is partially resorbed and located on a normal fetus. Ischiopagus which defines the parasitic twins connected from ileum is the rarest form of heteropagus abnormalities. In this case, a thirteen week old fetus was diagnosed with ischiopagus, ambiguous genitalia, and left kidney agenesis during the first trimester ultrasonography screening. Termination was applied with the family decision. These cases should be evaluated together with accompanying multisystem anomalies. Informing the family with details about the viability of the fetus is important to prevent unnecessary termination. | |
dc.identifier.citation | AKAR, B., HAGVERDIYEV, E., ASLANCAN, R., GÜMÜŞTAŞ, G., CALISKAN, E. (2020). Ischiopagus Which is the Rarest Form of Heteropagus Along With Ambiguous Genitalia and Kidney Agenesis: A Case Report. Ege Klinikleri Tıp Dergisi , 58(2), 223 - 226. | |
dc.identifier.endpage | 226 | |
dc.identifier.issn | 2148-0990 | |
dc.identifier.issue | 2 | |
dc.identifier.startpage | 223 | |
dc.identifier.trdizinid | 485158 | |
dc.identifier.uri | https://search.trdizin.gov.tr/tr/yayin/detay/485158/ischiopagus-which-is-the-rarest-form-of-heteropagus-along-with-ambiguous-genitalia-and-kidney-agenesis-a-case-report | |
dc.identifier.uri | https://hdl.handle.net/20.500.12713/6748 | |
dc.identifier.volume | 58 | |
dc.indekslendigikaynak | TR-Dizin | |
dc.institutionauthor | Akar, Bertan | |
dc.institutionauthorid | Bertan Akar / 0000-0003-0494-6867 | |
dc.language.iso | en | |
dc.publisher | İzmir Hastaneline Yardım ve Bilimsel Araştırmaları Teşvik Derneği | |
dc.relation.ispartof | Ege Klinikleri Tıp Dergisi | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | Heteropagus | |
dc.subject | kidney agenesis | |
dc.subject | ambiguous genitalia | |
dc.title | Ischiopagus Which is the Rarest Form of Heteropagus Along With Ambiguous Genitalia and Kidney Agenesis: A Case Report | |
dc.title.alternative | Ambiguus Genitalya ve Böbrek Agenezisi ile Birlikte Görülen Heterofagusun en Nadir Formu Olan İskiofagus Vakası | |
dc.type | Article |
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