Roy E P, Gutmann L, Riggs J E
Department of Neurology, West Virginia University School of Medicine, Morgantown.
Muscle Nerve. 1989 Jan;12(1):52-5. doi: 10.1002/mus.880120110.
Motor conduction studies were performed serially in 10 patients, ages 10-62 years, with clinical and electrophysiological criteria of hereditary motor and sensory neuropathy type 1 (HMSN-1) over periods of 11-19 years. Median nerve conduction velocity (MNCV) and distal motor latency showed no significant change on serial studies. Mean median compound muscle action potential (CMAP) amplitude values, however, decreased 66% in 8 patients. Observed clinical progression in HMSN-1, over prolonged periods of time, was not associated with MNCV slowing. However, CMAP amplitude reduction, reflecting progressive axonal loss, correlated with clinical deterioration.
对10名年龄在10至62岁之间、符合1型遗传性运动和感觉神经病(HMSN - 1)临床及电生理标准的患者进行了长达11至19年的系列运动传导研究。在系列研究中,正中神经传导速度(MNCV)和远端运动潜伏期无显著变化。然而,8名患者的平均正中复合肌肉动作电位(CMAP)幅度值下降了66%。在较长时间内观察到的HMSN - 1临床进展与MNCV减慢无关。然而,反映进行性轴突丢失的CMAP幅度降低与临床恶化相关。