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《整形外科学》

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

发表时间:2015-12-08  浏览次数:1334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:

其他外文数据库

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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