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Eur J Paediatr Dent
; 17(4): 315-317, 2016 Dec.
Article
in English
| MEDLINE
| ID: mdl-28045321
ABSTRACT
BACKGROUND: 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-dento-facial phenotypes, along with a review of the literature.