Type 1 Crouzon syndrome with headache

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dc.authorscopusid36476952800
dc.authorscopusid8678198300
dc.authorscopusid50161005400
dc.authorscopusid55675860600
dc.authorscopusid36055987800
dc.authorscopusid15764379200
dc.authorscopusid35867258900
dc.contributor.authorArica, Vefik
dc.contributor.authorTutanç, Murat
dc.contributor.authorBayaro?ullari, Hanifi
dc.contributor.authorGünher Arica, Seç
dc.contributor.authorBaşarslan, Fatmagül
dc.contributor.authorDavran, Ramazan
dc.contributor.authorKorkmaz, Inan
dc.date.accessioned2024-09-19T15:43:36Z
dc.date.available2024-09-19T15:43:36Z
dc.date.issued2013
dc.departmentHatay Mustafa Kemal Üniversitesien_US
dc.description.abstractCrouzon syndrome defined by French neurosurgeon Crouzon in 1912. Crouzon syndrome which is characterized by craniosynostosis and dysmorphic facial appearance. This autosomal dominant disease has an incidence rate of 16/1,000,000. Craniosynostosis premature closure of cranial sutures, results in craniofacial anomalies. 4.5% of cases with craniosynostosis have Crouzon syndrome. Craniosynostosis can occur in utero or in the first three years of life. It rarely occurs later. Phenotypically specific types of craniosynostosis have been linked to fibroblast growth factor receptor gene (FGFR) mutations. Clinical findings of Crouzon, Apert and Pfeifer syndromes are secondary to FGFR-2 gene mutations. In Crouzon syndrome brachycephaly, ptosis, exophthalmos, hypertelorism, acanthosis nigricans, rostrate type nose, ear and palate anomalies can occur of as a result of premature closure of cranial sutures. In this report we present a 5 years old male with headache. He has Crouzon Syndrome and beaten copper appearance in craniography.en_US
dc.identifier.endpage112en_US
dc.identifier.issn1305-2381
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-84877128622en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage110en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12483/14442
dc.identifier.volume9en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.relation.ispartofNobel Medicusen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAortic arch anomalyen_US
dc.subjectMagnetic resonance angiographyen_US
dc.subjectVertebral artery anomalyen_US
dc.titleType 1 Crouzon syndrome with headacheen_US
dc.title.alternativeBaş a?risi nedeni?yle başvuran ti?p 1 Crouzon sendromuen_US
dc.typeArticleen_US

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