Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/68137
Type: Artigo de periódico
Title: Goldenhar syndrome: clinical features with orofacial emphasis
Author: Martelli, H
de Miranda, RT
Fernandes, CM
Bonan, PRF
Paranaiba, LMR
Graner, E
Coletta, RD
Abstract: Objectives: Goldenhar syndrome (GS) is a relatively common developmental disorder characterized by craniofacial anomalies in association with vertebral, cardiac, renal, and central nervous system defects. This paper describes GS features with special emphasis on oral characteristics. Material and Methods: The clinical features of 6 patients with GS aged 3 months to 12 years are described, and a brief review of the literature about this genetic disorder is presented. Results: All patients demonstrated the classical triad of GS, including mandibular hypoplasia resulting in facial asymmetry, ear and/or eye malformation, and vertebral anomalies. In addition, renal and gastrointestinal abnormalities were observed in 2 patients. Regarding the oral involvement, 2 patients presented cleft lip and palate, and 1 patient had temporomandibular joint malformation. Malocclusion was found in all patients. Conclusion: Our orofacial findings correlate with the reported cases in the literature, and point out that after diagnosis GS patients need to be examined for systemic abnormalities.
Subject: Goldenhar syndrome
Mandible
Facial asymmetry
Country: Brasil
Editor: Univ Sao Paulo Fac Odontologia Bauru
Rights: fechado
Identifier DOI: 10.1590/S1678-77572010000600019
Date Issue: 2010
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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