Literature DB >> 17466880

Intraoral features of Apert's syndrome.

Ariadne Letra1, Ana Lúcia Pompéia Fraga de Almeida, Rosane Kaizer, Luis Augusto Esper, Silvia Sgarbosa, José Mauro Granjeiro.   

Abstract

OBJECTIVE: To evaluate the intraoral features of patients with Apert's syndrome in treatment at the Hospital of Rehabilitation and Craniofacial Anomalies of University of São Paulo (HRAC-USP), a national reference center for treatment of craniofacial anomalies in Brazil. STUDY
DESIGN: In this retrospective study, of 56,000 patients registered at HRAC-USP, 36 patients were diagnosed with Apert's syndrome and were either examined or had their medical files evaluated, aiming to characterize lip posture, mouth shape, maxillary hypoplasia, palatal morphology, dental anomalies, and malocclusion.
RESULTS: Most patients were characterized as mouth breathers for presenting with hypotonic lips and trapezoidal-shaped mouths. Other frequent findings were the presence of highly arched palates and hypoplastic maxilla, with gingival lateral swellings that increased in size with age. Crowding of teeth and malocclusion were commonly observed, and cases of hypodontia were frequent. Contrary to previous studies demonstrating a high incidence of cleft soft palate, in this study only 1 of 23 patients presented a true cleft.
CONCLUSIONS: The intraoral features of patients with Apert's syndrome in the population studied match most of the findings in other populations. However, the occurrence of cleft soft palate was unexpectedly low and morphologically normal teeth were found. In addition, hypodontia was frequently observed. Variations in frequency of observations of some characteristics might be related to differences in sample size or population.

Entities:  

Mesh:

Year:  2006        PMID: 17466880     DOI: 10.1016/j.tripleo.2006.04.006

Source DB:  PubMed          Journal:  Oral Surg Oral Med Oral Pathol Oral Radiol Endod        ISSN: 1079-2104


  14 in total

1.  Treatment timing and multidisciplinary approach in Apert syndrome.

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2.  Guideline for Care of Patients With the Diagnoses of Craniosynostosis: Working Group on Craniosynostosis.

Authors:  Irene M J Mathijssen
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4.  Cranio-maxillofacial, orthodontic and dental treatment in three patients with Apert syndrome.

Authors:  S Carpentier; J Schoenaers; C Carels; A Verdonck
Journal:  Eur Arch Paediatr Dent       Date:  2014-03-19

5.  Apert Syndrome: Late presentation and treatment challenges.

Authors:  Abdelmoneim E M Kheir; Ahlam A Hamed; Wala M Maki; Lina H M Hasan
Journal:  Sudan J Paediatr       Date:  2014

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Authors:  B Vadiati Saberi; A Shakoorpour
Journal:  J Dent (Tehran)       Date:  2011-06-30

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Review 8.  From Bench to Bedside and Back: Improving Diagnosis and Treatment of Craniofacial Malformations Utilizing Animal Models.

Authors:  Alice F Goodwin; Rebecca Kim; Jeffrey O Bush; Ophir D Klein
Journal:  Curr Top Dev Biol       Date:  2015-10-06       Impact factor: 4.897

9.  Fuz mutant mice reveal shared mechanisms between ciliopathies and FGF-related syndromes.

Authors:  Jacqueline M Tabler; William B Barrell; Heather L Szabo-Rogers; Christopher Healy; Yvonne Yeung; Elisa Gomez Perdiguero; Christian Schulz; Basil Z Yannakoudakis; Aida Mesbahi; Bogdan Wlodarczyk; Frederic Geissmann; Richard H Finnell; John B Wallingford; Karen J Liu
Journal:  Dev Cell       Date:  2013-06-24       Impact factor: 12.270

10.  Comparison of periodontal parameters in individuals with syndromic craniosynostosis.

Authors:  Paula Simões Múfalo; Rosane de Oliveira Fortes Kaizer; Gisele da Silva Dalben; Ana Lúcia Pompéia Fraga de Almeida
Journal:  J Appl Oral Sci       Date:  2009 Jan-Feb       Impact factor: 2.698

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