A case of Beckwith- Wiedemann syndrome with peculiar dental findings

Callea M.Yavuz I.Clarich G.Gunay A.Vinciguerra A.Unal M.Sahbaz C.2024-04-242024-04-2420161591-996Xhttps://hdl.handle.net/11468/24996Background 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.eninfo:eu-repo/semantics/closedAccessBeckwith Wiedemann SyndromeMouthOral ManifestationsSystemic ManifestationsA case of Beckwith- Wiedemann syndrome with peculiar dental findingsA case of Beckwith- Wiedemann syndrome with peculiar dental findingsArticle1743153172-s2.0-8500998615528045321Q1