Pathology in metopic synostosis

dc.contributor.authorKarabagli, Pinar
dc.date.accessioned2020-03-26T18:42:49Z
dc.date.available2020-03-26T18:42:49Z
dc.date.issued2013
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractPremature closure and subsequent ossification of the metopic suture results in triangular head shape called trigonocephaly and is characterized by a midline metopic ridge, frontotemporal narrowing, and an increased biparietal diameter. Trigonocephaly is the second most frequent type of craniosynostosis. It can be isolated and associated with other congenital anomalies without any known syndrome, or occurs as part of a multiple malformation syndrome. Improvement in treatment is directed by a thorough understanding of the basic pathology of this condition. This review aims to provide an overview of metopic synostosis by correlating what is known about pathogenesis and pathology of this entity.en_US
dc.identifier.doi10.1007/s00381-013-2284-4en_US
dc.identifier.endpage2170en_US
dc.identifier.issn0256-7040en_US
dc.identifier.issn1433-0350en_US
dc.identifier.issue12en_US
dc.identifier.pmid24092422en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage2165en_US
dc.identifier.urihttps://dx.doi.org/10.1007/s00381-013-2284-4
dc.identifier.urihttps://hdl.handle.net/20.500.12395/29713
dc.identifier.volume29en_US
dc.identifier.wosWOS:000327894900007en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherSPRINGERen_US
dc.relation.ispartofCHILDS NERVOUS SYSTEMen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectTrigonocephalyen_US
dc.subjectMetopic sutureen_US
dc.subjectPathologyen_US
dc.subjectCraniosynostosisen_US
dc.titlePathology in metopic synostosisen_US
dc.typeArticleen_US

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