Moebius Syndrome: A Case Report with Unique Features

Divya Ramraika, Pradeep Kumar, Bithi Chowdhury
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引用次数: 0

Abstract

We report a case of a 13-year-old female who presented in the medical emergency with seizures and was referred to the ophthalmology department for fundus examination. On examination, she was found to have bilateral asymmetric VIth and VIIth nerve palsy, bilateral horizontal gaze paresis (right > left), tongue atrophy, mask-like face, normal intelligence, prominent lower lip, and history of treated club foot. She was diagnosed to have Moebius syndrome based on the above findings. She also had some atypical features such as head tilt, significant refractive error, anisometric amblyopia, and horizontal nystagmus. Her computed tomography scan of the head revealed neurocysticercosis.
莫比斯综合征:一例独特的报告
我们报告一例13岁的女性谁提出了医疗紧急癫痫发作,并被转介到眼科进行眼底检查。检查发现双侧不对称VIth和VIth神经麻痹,双侧水平凝视性麻痹(右>左),舌萎缩,面具样脸,智力正常,下唇突出,治疗过内翻足。根据上述结果,她被诊断为莫比乌斯综合征。她也有一些不典型的特征,如头部倾斜、明显的屈光不正、屈光参差性弱视和水平眼震。她的头部计算机断层扫描显示神经囊虫病。
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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