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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Main Authors: B. Vadiati Saberi, A. Shakoorpour
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2011-06-01
Series:Frontiers in Dentistry
Subjects:
Online Access:https://jdt.tums.ac.ir/index.php/jdt/article/view/248
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author B. Vadiati Saberi
A. Shakoorpour
author_facet B. Vadiati Saberi
A. Shakoorpour
author_sort B. Vadiati Saberi
collection DOAJ
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 doaj.art-488d626659d7473cb24e9b5701ecb3d62022-12-22T02:12:32ZengTehran University of Medical SciencesFrontiers in Dentistry2676-296X2011-06-0182Apert Syndrome: Report of a Case with Emphasis on Oral Manifestations B. Vadiati Saberi0 A. Shakoorpour1Postgraduate Student, Department of Periodontology, School of Dentistry, Babol University of MedicalPostgraduate Student, Department of Periodontology, School of Dentistry, Babol University of MedicalTo 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.https://jdt.tums.ac.ir/index.php/jdt/article/view/248Tooth AbnormalitiesMouth AbnormalitiesTooth EruptionEctopicCraniosynostoses
spellingShingle B. Vadiati Saberi
A. Shakoorpour
Apert Syndrome: Report of a Case with Emphasis on Oral Manifestations
Frontiers in Dentistry
Tooth Abnormalities
Mouth Abnormalities
Tooth Eruption
Ectopic
Craniosynostoses
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 Tooth Abnormalities
Mouth Abnormalities
Tooth Eruption
Ectopic
Craniosynostoses
url https://jdt.tums.ac.ir/index.php/jdt/article/view/248
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