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运动神经元病(MND)罕见自发缓解。本文报道4例表现酷似肌萎缩侧索硬化(ALS)的患者,唯一不同之处是均获完全恢复或基本恢复。病例报告男3、女1例,年龄39～74岁。起病到达高峰的时间为6周～4个月。肢体无力为主要临床表现,3例为四肢无力,1例为双下肢无力,其中1例有颈肌无力。4例均有肌束颤动。3例有肢体肌肉萎缩,多见于肢体远端。3例有手足麻木或疼痛,1例检查有手指尖痛触
Motor neuron disease (MND) rare spontaneous remission. This article reports 4 patients who behave resembling amyotrophic lateral sclerosis (ALS) in patients, the only difference is that they have been completely recovered or basically recovered. Case report male 3, female 1 case, aged 39 to 74 years old. The onset of the peak time of 6 weeks to 4 months. Limb weakness as the main clinical manifestations, 3 cases of limb weakness, 1 case of weakness of both lower extremities, 1 case of cervical muscle weakness. 4 cases had fasciculation. 3 cases of limb muscle atrophy, more common in the distal limbs. 3 patients had hand, foot numbness or pain, and 1 patient had a touch of a finger pain