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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Format: | Article |
Language: | English |
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Wolters Kluwer Medknow Publications
2010-01-01
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Series: | Contemporary Clinical Dentistry |
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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. |
first_indexed | 2024-12-19T20:43:18Z |
format | Article |
id | doaj.art-3a3be7a2436d4c59885561d5188090ba |
institution | Directory Open Access Journal |
issn | 0976-237X 0976-2361 |
language | English |
last_indexed | 2024-12-19T20:43:18Z |
publishDate | 2010-01-01 |
publisher | Wolters Kluwer Medknow Publications |
record_format | Article |
series | Contemporary Clinical Dentistry |
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 |