A case of Beckwith-Wiedemann syndrome with peculiar dental findings

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dc.contributor.authorCallea, M.
dc.contributor.authorYavuz, I.
dc.contributor.authorClarich, G.
dc.contributor.authorGunay, A.
dc.contributor.authorVinciguerra, A.
dc.contributor.authorUnal, M.
dc.contributor.authorSahbaz, C.
dc.date.accessioned2024-04-24T17:49:50Z
dc.date.available2024-04-24T17:49:50Z
dc.date.issued2016
dc.departmentDicle Üniversitesien_US
dc.description.abstractBackground Beckwith-Wiedemann syndrome (BINS, OMIM 130650) is a rare genetic disorder characterised by overgrowth, tumor predisposition and congenital malformations. Few systemic manifestations and oral features have been reported so far. Case report We report on a case of BWS, describing all features expanding the knowledge on oro-dentofacial phenotypes, along with a review of the literature.en_US
dc.identifier.endpage317en_US
dc.identifier.issn1591-996X
dc.identifier.issn2035-648X
dc.identifier.issue4en_US
dc.identifier.pmid28045321
dc.identifier.startpage315en_US
dc.identifier.urihttps://hdl.handle.net/11468/23003
dc.identifier.volume17en_US
dc.identifier.wosWOS:000392570500012
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.language.isoenen_US
dc.publisherAriesdue Srlen_US
dc.relation.ispartofEuropean Journal of Paediatric Dentistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBeckwith Wiedemann Syndromeen_US
dc.subjectMouthen_US
dc.subjectOral Manifestationsen_US
dc.subjectSystemic Manifestationsen_US
dc.titleA case of Beckwith-Wiedemann syndrome with peculiar dental findingsen_US
dc.titleA case of Beckwith-Wiedemann syndrome with peculiar dental findings
dc.typeArticleen_US

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