To Report a Rare Case of Goldenhar Syndrome

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 bilateral involvement. The clinical features of this patient with GS aged 22 are described, and a brief review of the literature about this genetic disorder is also presented.