戈登哈尔综合征并发下颌畸形和单侧腭裂。

Hao Chen,Weimin Shen
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引用次数: 0

摘要

戈登哈尔综合征(Goldenhar Syndrome)又称眼耳畸形(occulo-auriculo-vertebral spectrum,OAVS)或半面神经小畸形(hemifacial microsomia,HFM),其特征是眼睛、耳朵、上颚、下颚、上腭和脊柱等结构的发育异常。面部畸形主要源于支弓畸形,有时被归类为第一和第二支弓综合征。据估计,其发病率约为 3500 分之 1。在此,作者介绍了一例 10 个月大的戈登哈尔综合征男婴,这是一种特别独特的腭裂表现,我们采用了肌粘膜瓣重建软腭。
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Goldenhar Syndrome Complicated by Hemifacial Microsomia and Unilateral Cleft Palate Absence.
Goldenhar syndrome, also known as oculo-auriculo-vertebral spectrum (OAVS) or hemifacial microsomia (HFM), is characterized by developmental anomalies in structures such as the eyes, ears, upper jaw, lower jaw, upper palate, and spine. The facial abnormalities, stemming predominantly from branchial arch malformation, are sometimes categorized as the first and second branchial arch syndromes. Its incidence is estimated to be ∼1 in 3500. Here, the authors present a case of Goldenhar syndrome in a male infant at the age of 10 months, showcasing a particularly unique manifestation of cleft palate, for which we employed myomucosal flap reconstruction of the soft palate.
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