A case of goldenhar's syndrome
Authors : A. Atabey, A. Barutçu
Pages : 67-70
View : 11 | Download : 9
Publication Date : 1992-04-01
Article Type : Research
Abstract :Goldenhar's syndrome (Goldenhar-Gorlin syndrome, facioauricuiovertebral sequence, oculoauriculoverteb- ral dysplasia) is a variant of craniofacial microsomia (first and second branchial arch syndrome). It is generally characterized by epibulbar dermoids and/or lipo- dermoids, pretragal blinded fistulas, skin tags on the cheek and vertebral anomalies. A 24-year-old female patient with Goldenhar's syndrome was presented in this paper.Keywords : Craniofacial anomalies - Facial abnormalities - Goldenhar's syndrome