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Apert Syndrome: Report of a Case with Emphasis on Oral Manifestations

To report the oral findings, including dental anomalies, ectopic eruption of the maxillary permanent first molars and periodontal disease and soft tissue alterations, in a subject with Apert syndrome. Clinical and radiographic examination of a patient with Apert syndrome, aged 21 years old, not prev...

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Detalles Bibliográficos
Autores principales: Vadiati Saberi, B., Shakoorpour, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184741/
https://www.ncbi.nlm.nih.gov/pubmed/21998814
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author Vadiati Saberi, B.
Shakoorpour, A.
author_facet Vadiati Saberi, B.
Shakoorpour, A.
author_sort Vadiati Saberi, B.
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description To report the oral findings, including dental anomalies, ectopic eruption of the maxillary permanent first molars and periodontal disease and soft tissue alterations, in a subject with Apert syndrome. Clinical and radiographic examination of a patient with Apert syndrome, aged 21 years old, not previously submitted for orthodontic or orthognathic treatment. Dental anomalies were present in a patient. Intraoral evaluation revealed poor oral hygiene with varying degrees of periodontal involvement, an arched swelling (pseudo cleft configuration), class III malocclusion, anterior open bite, posterior crossbite, supernumerary teeth, ectopic eruption and creamy white enamel opacities, an excessively large appearing tongue and a v-shaped maxillary arch. The occurrence of typical lateral palatal swellings agrees with the literature. The high prevalence of dental anomalies and ectopic eruption may suggest a possible etiologic relationship with the syndrome.
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spelling pubmed-31847412011-10-13 Apert Syndrome: Report of a Case with Emphasis on Oral Manifestations Vadiati Saberi, B. Shakoorpour, A. J Dent (Tehran) Case Report To report the oral findings, including dental anomalies, ectopic eruption of the maxillary permanent first molars and periodontal disease and soft tissue alterations, in a subject with Apert syndrome. Clinical and radiographic examination of a patient with Apert syndrome, aged 21 years old, not previously submitted for orthodontic or orthognathic treatment. Dental anomalies were present in a patient. Intraoral evaluation revealed poor oral hygiene with varying degrees of periodontal involvement, an arched swelling (pseudo cleft configuration), class III malocclusion, anterior open bite, posterior crossbite, supernumerary teeth, ectopic eruption and creamy white enamel opacities, an excessively large appearing tongue and a v-shaped maxillary arch. The occurrence of typical lateral palatal swellings agrees with the literature. The high prevalence of dental anomalies and ectopic eruption may suggest a possible etiologic relationship with the syndrome. Tehran University of Medical Sciences 2011 2011-06-30 /pmc/articles/PMC3184741/ /pubmed/21998814 Text en Copyright © Dental Research Center, Tehran University of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0), which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Case Report
Vadiati Saberi, B.
Shakoorpour, A.
Apert Syndrome: Report of a Case with Emphasis on Oral Manifestations
title Apert Syndrome: Report of a Case with Emphasis on Oral Manifestations
title_full Apert Syndrome: Report of a Case with Emphasis on Oral Manifestations
title_fullStr Apert Syndrome: Report of a Case with Emphasis on Oral Manifestations
title_full_unstemmed Apert Syndrome: Report of a Case with Emphasis on Oral Manifestations
title_short Apert Syndrome: Report of a Case with Emphasis on Oral Manifestations
title_sort apert syndrome: report of a case with emphasis on oral manifestations
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184741/
https://www.ncbi.nlm.nih.gov/pubmed/21998814
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