Callea, M.Yavuz, I.Clarich, G.Gunay, A.Vinciguerra, A.Unal, M.Sahbaz, C.2024-04-242024-04-2420161591-996X2035-648Xhttps://hdl.handle.net/11468/23003Background 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.eninfo:eu-repo/semantics/closedAccessBeckwith Wiedemann SyndromeMouthOral ManifestationsSystemic ManifestationsArticle174315317WOS:00039257050001228045321Q4