A case of Beckwith-Wiedemann syndrome with peculiar dental findings.
Eur J Paediatr Dent
; 17(4): 315-317, 2016 Dec.
Article
en En
| 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.
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Bases de datos:
MEDLINE
Asunto principal:
Anomalías Dentarias
/
Síndrome de Beckwith-Wiedemann
Tipo de estudio:
Diagnostic_studies
Límite:
Child, preschool
/
Humans
/
Male
Idioma:
En
Revista:
Eur J Paediatr Dent
Asunto de la revista:
ODONTOLOGIA
/
PEDIATRIA
Año:
2016
Tipo del documento:
Article
País de afiliación:
Italia