Goldenhar Syndrome in a pediatric patient: a case report and review of literature / Síndrome de Goldenhar em um paciente infantil: relato de caso e revisão da literatura
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 13500 to 15600 live births, and a gender ratio of 32 (malefemale), presenting more frequently in children with congenitaldeafness. The purpose of this case report was to describe clinical presentation of Goldenhar syndrome in a five-year old male with no significant familyhistory, 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.