Meyer B U, Britton T C, Bischoff C, Machetanz J, Benecke R, Conrad B
Department of Neurology, Technical University, Munich, F.R.G.
Mov Disord. 1991;6(4):320-3. doi: 10.1002/mds.870060409.
Electromyographic (EMG) responses evoked by transcranial magnetic brain stimulation were studied in nine patients with Wilson's disease (WD). Six of the nine patients had prolonged central motor latencies (CMLs), reduced amplitude, or absent responses in at least one of the examined muscles. In one patient, abnormal EMG responses normalized following treatment with penicillamine. Pathophysiologically abnormal EMG responses might result from a potentially reversible impairment of corticomotoneuronal pathways and/or a reduced excitability of motoneurons due to basal ganglia dysfunction. The possible pathophysiological mechanisms are discussed.
对9例威尔逊病(WD)患者进行了经颅磁刺激诱发的肌电图(EMG)反应研究。9例患者中有6例在至少一块受检肌肉中出现中枢运动潜伏期(CML)延长、波幅降低或反应缺失。1例患者经青霉胺治疗后异常的肌电图反应恢复正常。病理生理学上,异常的肌电图反应可能源于皮质运动神经元通路潜在的可逆性损伤和/或由于基底神经节功能障碍导致的运动神经元兴奋性降低。文中讨论了可能的病理生理机制。