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.
|Number of pages||3|
|Journal||European journal of paediatric dentistry : official journal of European Academy of Paediatric Dentistry|
|Publication status||Published - Dec 2016|
- Journal Article