Goldenhar综合症

Advances in Ophthalmology & Visual System Pub Date : 2018-02-08 DOI:10.15406/aovs.2018.08.00265

A. Chauhan, S. Chauhan

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引用次数: 0

摘要

Goldenhar综合征是一种遗传性疾病，其特征是耳前附属物、球外皮样，以及心脏、肾脏、脊椎、中枢神经和胃肠道系统的异常。我们报告一个7岁男性患者的高登哈综合征，他表现为角膜缘皮样，耳前标签，小畸形和下颌发育不全。我们的目的是报告这个病例，考虑到这种综合征的罕见性，并在我们的病人看到经典的迹象。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Goldenhar Syndrome

Goldenhar syndrome is a hereditary condition which is characterized by preauricular appendages, epibulbar dermoids, along with anomalies of the heart, kidney, and vertebral, central nervous and gastrointestinal system. We report a case of Goldenhar syndrome in a 7-years-old male patient who presented with limbal dermoid, pre auricular tag, microtia and mandibular hypoplasia. We AIM to report this case, given the rarity of this syndrome, and classical signs seen in our patient.

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Advances in Ophthalmology & Visual System

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