Goldenhar Syndrome in a pediatric patient: a case report and review of literature

• Autor(a) principal: AGNOL,Mauro Antonio Dall
• Data de Publicação: 2016
• Outros Autores: BROWN,Amy Louise, THOMAZ,Luiz Alexandre, JUNQUEIRA,José Luiz Cintra, OLIVEIRA,Luciana Butini
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: RGO - Revista Gaúcha de Odontologia (Online)
• Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1981-86372016000400472
• topic: Craniofacial abnormalities; Diagnosis; Goldenhar syndrome

ABSTRACT Goldenhar Syndrome is a rare, generally sporadic condition, whose physical manifestations include asymmetric incomplete facial development, epibulbar dermoids, auricular malformations e auricular appendices, vertebral anomalies, central nervous system disturbances, ocular irregularities and visceral abnormalities. Its etiology is not fully understood, with its incidence ranging from 1:3500 to 1:5600 live births, and a gender ratio of 3:2 (male: female), presenting more frequently in children with congenital deafness. The purpose of this case report was to describe clinical presentation of Goldenhar syndrome in a five-year old male with no significant family history, where almost all of the classic signs of the condition were present. Considering its involvement in craniofacial structures, its rarity, and its wide spectrum of symptoms and associated systemic abnormalities, knowledge of this condition is paramount for the dental surgeon.