Prosthetic rehabilitation of a Crouzon patient: A case report

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 dent...

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Main Authors: Hanefi Kurt, Burç Gençel, Aydin C Kader
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2010-01-01
Series:Contemporary Clinical Dentistry
Subjects:
Online Access:http://www.contempclindent.org/article.asp?issn=0976-237X;year=2010;volume=1;issue=3;spage=196;epage=200;aulast=Kurt
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author Hanefi Kurt
Burç Gençel
Aydin C Kader
author_facet Hanefi Kurt
Burç Gençel
Aydin C Kader
author_sort Hanefi Kurt
collection DOAJ
description 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.
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spelling doaj.art-3a3be7a2436d4c59885561d5188090ba2022-12-21T20:06:20ZengWolters Kluwer Medknow PublicationsContemporary Clinical Dentistry0976-237X0976-23612010-01-011319620010.4103/0976-237X.72794Prosthetic rehabilitation of a Crouzon patient: A case reportHanefi KurtBurç GençelAydin C KaderCrouzon 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.http://www.contempclindent.org/article.asp?issn=0976-237X;year=2010;volume=1;issue=3;spage=196;epage=200;aulast=KurtCrouzon syndromeoverdentureprosthetic treatment
spellingShingle Hanefi Kurt
Burç Gençel
Aydin C Kader
Prosthetic rehabilitation of a Crouzon patient: A case report
Contemporary Clinical Dentistry
Crouzon syndrome
overdenture
prosthetic treatment
title Prosthetic rehabilitation of a Crouzon patient: A case report
title_full Prosthetic rehabilitation of a Crouzon patient: A case report
title_fullStr Prosthetic rehabilitation of a Crouzon patient: A case report
title_full_unstemmed Prosthetic rehabilitation of a Crouzon patient: A case report
title_short Prosthetic rehabilitation of a Crouzon patient: A case report
title_sort prosthetic rehabilitation of a crouzon patient a case report
topic Crouzon syndrome
overdenture
prosthetic treatment
url http://www.contempclindent.org/article.asp?issn=0976-237X;year=2010;volume=1;issue=3;spage=196;epage=200;aulast=Kurt
work_keys_str_mv AT hanefikurt prostheticrehabilitationofacrouzonpatientacasereport
AT burcgencel prostheticrehabilitationofacrouzonpatientacasereport
AT aydinckader prostheticrehabilitationofacrouzonpatientacasereport