A case of Beckwith-Wiedemann syndrome with peculiar dental findings
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Updated: Mar 9, 2026

Systematic Assessment of Mammalian Skull Specimens for Dental and Temporomandibular Joint Pathology
Published on: August 22, 2022
M Callea1, I Yavuz2, G Clarich3
1Unit of Dentistry, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
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.
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