A case of Beckwith-Wiedemann syndrome with peculiar dental findings

M Callea, Izzet Yavuz, G Clarich, A. Gunay, A Vinciguerra, Mehmet Unal, C. Sahbaz, M. Sinan Dogan, Francisco Cammarata-Scalisi

Research output: Contribution to journalArticlepeer-review


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.

Original languageEnglish
Pages (from-to)315-317
Number of pages3
JournalEuropean journal of paediatric dentistry : official journal of European Academy of Paediatric Dentistry
Issue number4
Publication statusPublished - Dec 2016


  • Journal Article


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