Mercelis R, Demeester J, Martin J J
J Neurol Neurosurg Psychiatry. 1980 Oct;43(10):888-96. doi: 10.1136/jnnp.43.10.888.
Two brothers presented with a slowly progressive scapuloperoneal syndrome starting in early childhood. Initially there were myopathic EMG changes, but these changed to those of denervation. Neuromuscular biopsies at an interval of five years confirmed the neurogenic character of the muscle atrophy.
两兄弟自幼起病,呈现缓慢进展的肩胛腓骨肌综合征。起初肌电图表现为肌病性改变,但后来转变为失神经改变。间隔五年进行的神经肌肉活检证实了肌肉萎缩的神经源性特征。