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Guillain-Barre Syndrome Presenting With Bilateral Facial Nerve Palsy

机译:格林-巴利综合症伴双侧面神经麻痹

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摘要

ObjectiveThis case study is about an 11-year-old girl with bilateral facial weakness, abnormal taste sensation, and absent deep tendon reflexes of both knees and ankles. However, the muscle power of the lower and upper extremities across all muscle groups was normal. After 2 days, she developed paresthesia and numbness in the lower extremities. Other neurologic examinations, such as fundoscopic evaluation of the retina were normal with the muscle power of both upper- and lower-extremities intact. A lumbar puncture revealed albumincytological dissociation. EMG and NCV were in favor of Guillain-Barre syndrome, for which IVIG was prescribed and the abnormal sensations in the lower limbs rapidly improved. Bilateral facial diplegia without weakness and paresthesia is a variant of Guillain-Barre syndrome that mostly presents with acute onset, rapid progression with or without limb weakness, paresthesia, and decreased or absent DTR and albumin-cytological dissociation.
机译:目的本案例研究涉及一个11岁的女孩,该女孩双侧面部无力,味觉异常且膝盖和脚踝的深部腱反射消失。但是,所有肌肉组的下肢和上肢的肌肉力量均正常。 2天后,她的下肢出现感觉异常和麻木。其他神经系统检查,例如眼底镜检查视网膜正常,上下肢肌肉力量均完好无损。腰椎穿刺显示白细胞分离。 EMG和NCV支持吉兰-巴雷综合症,为此开了IVIG,下肢异常感觉迅速得到改善。双侧面部两肢瘫痪无弱点和感觉异常是格林-巴利综合征的一种变体,主要表现为急性发作,快速进展,伴有或不伴有肢体无力,感觉异常,DTR和白蛋白细胞学解离减少或不存在。

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