Craniofacial abnormalities in goldenhar syndrome: a case report with review of the literature

发表时间：2015-12-08 浏览次数：1116次

引用：

Kumaresan R, Srinivasan B, Narayanan M, Cugati N, Karthikeyan P. Craniofacial ab

关键词：

作者：

Ramesh Kumaresan1, Balamanikanda Srinivasan1, Moha

作者单位：

1 Departments of Oral and Maxillofacial Surgery, F

出版年份：

2014

期刊页数：

108-113

收录者：

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摘要：

Goldenhar syndrome (oculo-auriculo-vertebral spectrum) is a rare congenital anomaly of unclear etiology and characterized by craniofacial anomalies such as hemifacial microsomia, auricular, ocular and vertebral anomalies. In many cases, this syndrome goes unnoticed due to a lack of knowledge about its features and because of its associated wide range of overlapping anomalies. Herewith, we present a case of Goldenhar syndrome in a 21-year-old male, who presented all the classical signs of this rare condition. This article also summarizes the characteristic features of patients with Goldenhar syndrome.

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