一例继发于早期运动神经元病的脊柱前凸（弯曲脊柱）病例。
A case of camptocormia (bent spine) secondary to early motor neuron disease.
作者信息
Feriha Ozer, Aytul Mutlu, Hasan Meral
机构信息
Department of Neurology, Haseki Research and Educational Hospital, Istanbul, Turkey.
出版信息
Behav Neurol. 2004;15(1-2):51-4. doi: 10.1155/2004/163957.
Abstract
Camptocormia is a gait disorder, characterized by hyperflexion of thoracolumbar spine which increases on walking, and disappears in the supine position. A 48 year-old man developed progressive gait deterioration for one year and slight weakness and tremor of both hands for five months. It eventually became apparent that the patient had motor neuron disease, as well as symptoms of extrapyramidal disorder.
摘要
弯腰驼背是一种步态障碍，其特征为胸腰椎过度前屈，在行走时加重，仰卧位时消失。一名48岁男性出现进行性步态恶化1年，双手轻微无力和震颤5个月。最终发现该患者患有运动神经元病以及锥体外系障碍症状。
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