ABSTRACT
Goldenhar’s syndrome is a rare congenital syndrome characterized with ear, cardiac, and vertebral anomalies, facial asymmetria, epibulbar and dermoid cysts. The incidence is around 1/5600 a live birth. The patients with Goldenhar’s syndrome may refer with minor or major abnormalities. In this paper we report the clinical and laboratory findings of a patient with Goldenhar’s syndrome.