A rare case of goldenhar syndrome

Mamta Singaram, Praveen Ganesh Natarajan, Naryanamurthy Sundaramurthy, Alagar Raja Durairaj
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Abstract

Goldenhar syndrome is a rare congenital deformity involving a classical triad of auricular and ocular defects with hemifacialmicrosomia. Its etiology is unknown and various hypotheses have been highlighted in this article. The syndrome is often overlooked since it shares many distinctive features with other similar syndrome. This article highlights the features of Goldenhar syndrome and also discusses on the variant of this syndrome. Cleft palate is also an associated feature and the management of this two year old child is presented in detail in this article.
罕见的高氏综合征病例
Goldenhar综合征是一种罕见的先天性畸形,涉及典型的耳部和眼部缺陷三联征,并伴有半面小畸形。其病因不明,各种假说已在文章中强调。这种综合征经常被忽视,因为它与其他类似综合征有许多独特的特征。本文着重介绍了高氏综合征的特点,并对其变型进行了探讨。腭裂也是一种相关特征,本文将详细介绍这两岁儿童的治疗方法。
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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