Goldston Syndrome; Diagnosis of Multiple Fetal Anomaliesaaa

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dc.authorid0000-0002-3089-3159
dc.authorwosidKAYA, SINEM ALBAYRAK/AAV-4753-2021
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.departmentFakülteler, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Kadın Hastalıkları ve Doğum Ana Bilim Dalı
dc.description21st European Congress of Perinatal Medicine -- SEP 10-13, 2008 -- Istanbul, TURKEY
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.
dc.identifier.endpage+
dc.identifier.isbn978-88-7587-482-7
dc.identifier.startpage53
dc.identifier.urihttps://hdl.handle.net/20.500.11776/8239
dc.identifier.wosWOS:000272171800010
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.institutionauthorBozkurt, Serpil
dc.language.isoen
dc.publisherMedimond S R L
dc.relation.ispartofProceedings of the Xxi European Congress of Perinatal Medicine
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectDandy-Walker Malformation
dc.subjectKidneys
dc.titleGoldston Syndrome; Diagnosis of Multiple Fetal Anomaliesaaa
dc.typeConference Object

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