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Oral findings in Williams-Beuren syndrome.
Ferreira, S-B-P; Viana, M-M; Maia, N-G-F; Leão, L-L; Machado, R-A; Coletta, R-D; de Aguiar, M-J-B; Martelli-Júnior, H.
Afiliação
  • Ferreira SB; Health Science Program, State University of Montes Claros, Av. Cula Mangabeira 562 - Santo Expedito, Montes Claros - MG, 39401-001 Montes Claros - Minas Gerais - Brazil, shirle.ferreira@yahoo.com.br.
Med Oral Patol Oral Cir Bucal ; 23(1): e1-e6, 2018 Jan 01.
Article em En | MEDLINE | ID: mdl-29274148
ABSTRACT

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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Dentárias / Anormalidades Múltiplas / Síndrome de Williams / Má Oclusão Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Dentárias / Anormalidades Múltiplas / Síndrome de Williams / Má Oclusão Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article