Fraser syndrome: Two cases report

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dc.contributor.authorKilinç N.
dc.contributor.authorEtem H.
dc.date.accessioned2024-04-24T18:43:37Z
dc.date.available2024-04-24T18:43:37Z
dc.date.issued2007
dc.departmentDicle Üniversitesien_US
dc.description.abstractFraser syndrome (cryptophthalmos syndactyly syndrome) is a rare autosomal recessive disorder. The main features are cryptophthalmos (hidden eye), ear, nose and skeletal malformations, syndactyly, laryngeal stenosis and malformation of the uro-genital system, lungs, liver and central nervous system. Renal anomalies (uni-or bilateral agenesis) occur in 85 per cent. These anomalies were first documented by Fraser in 1962. Two Fraser syndrome cases diagnosed as normal spontan vaginal post delivery without prenatal following were presented rarely in the light of the literature knowledge.en_US
dc.identifier.endpage62en_US
dc.identifier.issn1016-5126
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-34347373729en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage59en_US
dc.identifier.urihttps://hdl.handle.net/11468/24225
dc.identifier.volume21en_US
dc.indekslendigikaynakScopus
dc.language.isotren_US
dc.relation.ispartofJinekoloji ve Obstetrik Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAutopsyen_US
dc.subjectCryptophthalmosen_US
dc.subjectFraser Syndromeen_US
dc.subjectSyndactylyen_US
dc.titleFraser syndrome: Two cases reporten_US
dc.title.alternativeFraser sendromu: İki olgu bildirimien_US
dc.typeArticleen_US

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