Syndromic craniosynostosis: A review

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dc.contributor.authorCammarata-Scalisi F.
dc.contributor.authorOzen B.
dc.contributor.authorChacín J.A.
dc.contributor.authorYavuz I.
dc.contributor.authorCallea M.
dc.date.accessioned2024-04-24T18:45:58Z
dc.date.available2024-04-24T18:45:58Z
dc.date.issued2016
dc.departmentDicle Üniversitesien_US
dc.description.abstractCraniosynostosisis a defect of the skull caused by premature fusion of one or more cranial sutures. It may be isolated finding or part of a syndrome and affects 1 in every 2,500 live births.Usually multiple sutures are involved and correspond in at least 20% of the cases. Syndromic craniosynostosis can be associated with various dysmorphic features involving the face, skeleton and nervous system. More than 180 syndromes have been reported with craniosynostosis.The aim of this review is to present the clinical and genetic characteristics of the most common types of syndromiccraniosynostosis.en_US
dc.identifier.endpage266en_US
dc.identifier.issn1309-100X
dc.identifier.issue3en_US
dc.identifier.scopus2-s2.0-85014009708
dc.identifier.scopusqualityQ3
dc.identifier.startpage262en_US
dc.identifier.urihttps://hdl.handle.net/11468/24994
dc.identifier.volume9en_US
dc.indekslendigikaynakScopus
dc.language.isoenen_US
dc.publisherUniversity of Dicleen_US
dc.relation.ispartofJournal of International Dental and Medical Research
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectClinicalen_US
dc.subjectCraniosynostosisen_US
dc.subjectGeneticsen_US
dc.subjectSyndromic Craniosynostosisen_US
dc.titleSyndromic craniosynostosis: A reviewen_US
dc.titleSyndromic craniosynostosis: A review
dc.typeArticleen_US

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