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Oral findings in Williams-Beuren syndrome

BACKGROUND: Williams-Beuren syndrome (WBS; OMIM #194050) is a developmental disorder characterized by congenital heart disease, intellectual disability, dysmorphic facial features and ophthalmologic abnormalities. Oral abnormalities are also described in clinical manifestations of the disease. This...

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Detalles Bibliográficos
Autores principales: Ferreira, Shirlene-Barbosa-Pimentel, Viana, Melissa-Machado, Maia, Naiara-Gonçalves-Fonseca, Leão, Letícia-Lima, Machado, Renato-Assis, Coletta, Ricardo-Della, de Aguiar, Marcos-José-Burle, Martelli-Júnior, Hercílio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medicina Oral S.L. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5822531/
https://www.ncbi.nlm.nih.gov/pubmed/29274148
http://dx.doi.org/10.4317/medoral.21834
Descripción
Sumario:BACKGROUND: Williams-Beuren syndrome (WBS; OMIM #194050) is a developmental disorder characterized by congenital heart disease, intellectual disability, dysmorphic facial features and ophthalmologic abnormalities. Oral abnormalities are also described in clinical manifestations of the disease. This paper describes orofacial features in patients with WBS. MATERIAL AND METHODS: Seventeen patients with a confirmed molecular diagnosis of WBS were examined for oral abnormalities through clinical oral evaluations and panoramic radiography. RESULTS: Malocclusion, specifically with dental midline deviation, and high-arched palate were the most common findings. CONCLUSIONS: The present results contribute to knowledge on the orofacial manifestations of WBS. Since such patients with WBS may develop severe oral abnormalities, early detection and treatment can help improve their quality of life. Key words:Congenital abnormalities, Orofacial features, Williams-Beuren syndrome.