A case of Beckwith- Wiedemann syndrome with peculiar dental findings

Basit Öğe Kaydı
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.accessioned2024-04-24T18:45:58Z
dc.date.available2024-04-24T18:45:58Z
dc.date.issued2016
dc.departmentDicle Üniversitesien_US
dc.description.abstractBackground Beckwith-Wiedemann syndrome (BWS, 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.issue4en_US
dc.identifier.pmid28045321
dc.identifier.scopus2-s2.0-85009986155
dc.identifier.scopusqualityQ1
dc.identifier.startpage315en_US
dc.identifier.urihttps://hdl.handle.net/11468/24996
dc.identifier.volume17en_US
dc.indekslendigikaynakScopus
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

Dosyalar

Koleksiyon

Scopus İndeksli Yayınlar Koleksiyonu
PubMed İndeksli Yayın Koleksiyonu