The “elfin face”: craniofacial and dental aspects of the Williams-Beuren syndrome.

Abstract:

: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.

authors

Maurino V,Azzi L,Vinci R,Croveri F,Boggio A,Silvestre-Rangil J,Tettamanti L,Tagliabue A

subject

Has Abstract

pub_date

2017-04-01 00:00:00

pages

105-111

issue

2 Suppl 1

eissn

0393-974X

issn

1724-6083

pii

13

journal_volume

31

pub_type

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