Prosthetic rehabilitation of a Crouzon patient: A case report
Identifieur interne : 004C29 ( Main/Merge ); précédent : 004C28; suivant : 004C30Prosthetic rehabilitation of a Crouzon patient: A case report
Auteurs : Hanefi Kurt ; Burç Gençel ; Aydin C. KaderSource :
- Contemporary Clinical Dentistry [ 0976-237X ] ; 2010.
Abstract
Crouzon syndrome is a rare genetic disorder, which can be defined as a variation of craniofacial dysostosis caused by the premature obliteration and ossification of two or more sutures. The growth pattern results in pseudoprognathism and malocclusions including an overcrowded or a widely spaced dentition. Specifically maxillary arch is narrow, high, and V-shaped. Cleft palate and bifid uvula are other possible features in the oral cavity. This report describes a non-surgical treatment model to overcome the remaining significant Class III intermaxillary relation and excessive tooth loss to recover function and aesthetics for a 25-year-old Crouzon patient.
Url:
DOI: 10.4103/0976-237X.72794
PubMed: 22114417
PubMed Central: 3220112
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Kader</name><affiliation><nlm:aff id="aff3"><italic>Private Practice, İstanbul University, Capa 34093, Istanbul, Turkey</italic></nlm:aff></affiliation></author></analytic><series><title level="j">Contemporary Clinical Dentistry</title><idno type="ISSN">0976-237X</idno><idno type="eISSN">0976-2361</idno><imprint><date when="2010">2010</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Crouzon syndrome is a rare genetic disorder, which can be defined as a variation of craniofacial dysostosis caused by the premature obliteration and ossification of two or more sutures. The growth pattern results in pseudoprognathism and malocclusions including an overcrowded or a widely spaced dentition. Specifically maxillary arch is narrow, high, and V-shaped. Cleft palate and bifid uvula are other possible features in the oral cavity. 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