Oral findings in patients with Apert Syndrome Achados bucais em pacientes com Síndrome de Apert

Oral findings in patients with Apert Syndrome Achados bucais em pacientes com Síndrome de Apert

INTRODUCTION: The Apert syndrome is a rare disorder of autosomal dominant inheritance caused by mutations in the FGFR2 gene at locus 10q26; patients with this syndrome present severe syndactyly, exophthalmia, ocular hypertelorism and hypoplastic midface with Class III malocclusion, besides systemic...

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Bibliographic Details
Main Authors: Gisele da Silva Dalben, Lucimara Teixeira das Neves, Marcia Ribeiro Gomide
Format: Article
Language:English
Published: University of São Paulo 2006-12-01
Series:Journal of Applied Oral Science
Subjects:
Anomalias dentárias
Alterações bucais
Irrupção dentária ectópica
Craniossinostose
Acrocefalosindactilia
Tooth abnormalities
Mouth abnormalities
Tooth eruption
ectopic
Craniosynostoses
Acrocephalosyndactylia
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1678-77572006000600014

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http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1678-77572006000600014

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