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Oral findings in Williams-Beuren syndrome

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Oral findings in Williams-Beuren syndrome

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dc.contributor.author Ferreira, Shirlene-Barbosa-Pimentel es
dc.contributor.author Viana, Melissa-Machado es
dc.contributor.author Maia, Naiara-Gonçalves-Fonseca es
dc.contributor.author Leão, Letícia Lima es
dc.contributor.author Machado, Renato Assis es
dc.contributor.author Della Coletta, Ricardo es
dc.contributor.author Burle Aguiar, Marcos José es
dc.contributor.author Martelli Júnior, Hercílio es
dc.date.accessioned 2018-05-02T12:37:39Z
dc.date.available 2018-05-02T12:37:39Z
dc.date.issued 2018 es
dc.identifier.citation Ferreira, Shirlene-Barbosa-Pimentel ; Viana, Melissa-Machado ; Maia, Naiara-Gonçalves-Fonseca ; Leão, Letícia Lima ; Machado, Renato Assis ; Della Coletta, Ricardo ; Burle Aguiar, Marcos José ; Martelli Júnior, Hercílio. Oral findings in Williams-Beuren syndrome. En: Medicina oral, patología oral y cirugía bucal. Ed. inglesa, 23 1 2018: 1- es
dc.identifier.uri http://hdl.handle.net/10550/65951
dc.description.abstract 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. Seventeen patients with a confirmed molecular diagnosis of WBS were examined for oral abnormalities through clinical oral evaluations and panoramic radiography. Malocclusion, specifically with dental midline deviation, and high-arched palate were the most common findings. 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. es
dc.title Oral findings in Williams-Beuren syndrome es
dc.type journal article es_ES
dc.subject.unesco UNESCO::CIENCIAS MÉDICAS es
dc.identifier.doi 10.4317/medoral.21834 es
dc.type.hasVersion VoR es_ES

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