A FRONTONASAL DYSPLASIA CASE WITH ABSENCE OF FALX CEREBRI

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dc.contributor.authorAltunhan, Hüseyin
dc.contributor.authorAnnagür, Ali
dc.contributor.authorÖzbek, Orhan
dc.contributor.authorÖrs, Rahmi
dc.date.accessioned2020-03-26T18:40:59Z
dc.date.available2020-03-26T18:40:59Z
dc.date.issued2013
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractFrontonasal dysplasia which is also called median cleft face syndrome, is a disease that presents with signs like hypertelorism, broad nasal base, formation defect of nasal edge, anterior cranium, bifidum ocultum, microphtalmia in the face and head but with possible anomalies in any organ or system. Central nervous system anomalies like corpus callosum agenesis, lipomas of corpus callosum and encephalosel may also be seen in these cases. We presented a frontonasal dysplasia case without falx cerebri. According to our investigation, this is the first case of frontonasal dysplasia without falx cerebri.en_US
dc.identifier.endpage117en_US
dc.identifier.issn1305-2381en_US
dc.identifier.issue1en_US
dc.identifier.startpage115en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12395/29146
dc.identifier.volume9en_US
dc.identifier.wosWOS:000318382500021en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isotren_US
dc.publisherNOBEL ILACen_US
dc.relation.ispartofNOBEL MEDICUSen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectFrontonasal dysplasiaen_US
dc.subjectmedian facial cleft syndromeen_US
dc.subjectnewbornen_US
dc.subjectcryptorchidismen_US
dc.subjectmicrophthalmiaen_US
dc.titleA FRONTONASAL DYSPLASIA CASE WITH ABSENCE OF FALX CEREBRIen_US
dc.typeArticleen_US

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