A case of goldenhar's syndrome
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
References
- Converse JM. Reconstructive Hastie Surgery. 2nd ed. Philadelphia: WB Saunders. 1977: 2146. 2360. 2408.
Details
Primary Language
English
Subjects
Clinical Sciences
Journal Section
Research Article
Publication Date
April 1, 1992
Submission Date
October 14, 2016
Acceptance Date
February 1, 1992
Published in Issue
Year 1992 Volume: 5 Number: 2