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dc.contributor.authorKaya, Mehmet Nur
dc.contributor.authorToprak, Ömer
dc.contributor.authorTurel, Sultan
dc.contributor.authorErgün, Uğur
dc.contributor.authorArslan, Taha Yasin
dc.date.accessioned2020-01-24T09:58:03Z
dc.date.available2020-01-24T09:58:03Z
dc.date.issued2019en_US
dc.identifier.issn2564-7784
dc.identifier.issn2564-7040
dc.identifier.urihttps://doi.org/10.5152/EurJTher.2019.600
dc.identifier.urihttps://hdl.handle.net/20.500.12462/10570
dc.descriptionToprak, Ömer (Balikesir Author)en_US
dc.description.abstractAbernethy malformation is a vascular congenital anomaly in which extrahepatic portocaval shunts develop. The patient was admitted to the gastroenterology department with complaints of abdominal pain and nausea. Ammonia and bilirubin levels were increased in the laboratory values and other liver function values were normal. The shunt was detected between the inferior vena cava and portal vein by ultrasonography and computed tomography, and the portal vein was hypoplastic. In this case report, we present a male patient diagnosed with Abernethy malformation type 2.en_US
dc.language.isoengen_US
dc.publisherAvesen_US
dc.relation.isversionof10.5152/EurJTher.2019.600en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAbdominal Painen_US
dc.subjectAbernethy Malformationen_US
dc.subjectCongenital Anomalyen_US
dc.titleCongenital extrahepatic portosystemic shunt: Abernethy malformation type 2en_US
dc.typearticleen_US
dc.relation.journalEuropean Journal of Therapeuticsen_US
dc.contributor.departmentTıp Fakültesien_US
dc.contributor.authorID0000-0002-2865-1687en_US
dc.identifier.volume25en_US
dc.identifier.issue3en_US
dc.identifier.startpage230en_US
dc.identifier.endpage232en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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