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dc.contributor.authorAbalı, Remzi
dc.contributor.authorAlbayrak Kaya, Sinem
dc.contributor.authorBozkurt, Serpil
dc.contributor.authorLeblebici, Cem
dc.contributor.authorYurtsever, Çiğdem Yavuz
dc.date.accessioned2022-05-11T14:35:49Z
dc.date.available2022-05-11T14:35:49Z
dc.date.issued2008
dc.identifier.isbn978-88-7587-482-7
dc.identifier.urihttps://hdl.handle.net/20.500.11776/8239
dc.description21st European Congress of Perinatal Medicine -- SEP 10-13, 2008 -- Istanbul, TURKEYen_US
dc.description.abstractGoldston syndrome is a multisystemic disorder characterised by polycystic kidneys with Dandy Walker malformation. The aim of our study is to report this rare case. We diagnosed cleft palate, micrognatia, dilatation of the fourth ventricle, total agenesis of corpus callosum, multicystic kidneys, club foot by ultrasound in the 23(th) week of gestation. Based on the findings of neonatal autopsy, fetus is proposed to be diagnose as Goldston syndrome. The etiology of this kind of familial disorder remains unclear, but a genetic factor might be involved.en_US
dc.language.isoengen_US
dc.publisherMedimond S R Len_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDandy-Walker Malformationen_US
dc.subjectKidneysen_US
dc.titleGoldston Syndrome; Diagnosis of Multiple Fetal Anomaliesaaaen_US
dc.typeproceedingPaperen_US
dc.relation.ispartofProceedings of the Xxi European Congress of Perinatal Medicineen_US
dc.departmentFakülteler, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Kadın Hastalıkları ve Doğum Ana Bilim Dalıen_US
dc.authorid0000-0002-3089-3159
dc.identifier.startpage53en_US
dc.identifier.endpage+en_US
dc.institutionauthorBozkurt, Serpil
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.authorwosidKAYA, SINEM ALBAYRAK/AAV-4753-2021
dc.identifier.wosWOS:000272171800010en_US


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