THE 'ELFIN FACE': CRANIOFACIAL AND DENTAL ASPECTS OF THE WILLIAMS-BEUREN SYNDROME
Autor: | V, Maurino, L, Azzi, R, Vinci, F, Croveri, A, Boggio, J, Silvestre-Rangil, L, Tettamanti, A, Tagliabue |
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Rok vydání: | 2017 |
Předmět: | |
Zdroj: | JOURNAL OF BIOLOGICAL REGULATORS AND HOMEOSTATIC AGENTS r-FISABIO: Repositorio Institucional de Producción Científica Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO) r-FISABIO. Repositorio Institucional de Producción Científica instname |
ISSN: | 0393-974X |
Popis: | Williams Syndrome is a rare congenital disorder characterized by supravalvular aortic stenosis, peripheral pulmonary artery stenosis, mental retard and dysmorfic facial features. As regards the dental aspects of the syndrome, the deletion of the elastin gene induced clinicians to suspect periodontal alterations with a greater frequency of gingivo-periodontitis, but on the contrary no association between the syndrome and periodontal diseases have been found. Furthermore, patients show a higher frequency of teeth hypoplasia, an abnormal tooth morphology during primary dentition (12.5%) and during permanent dentition. We present a case report of a 12-year-old Caucasian boy affected by Williams-Beuren Syndrome who visited our hospital for a dental and orthodontic evaluation. |
Databáze: | OpenAIRE |
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