Scaioli V, Pareyson D, Avanzini G, Sghirlanzoni A
Department of Neurophysiopathology, Istituto Nazionale Neurologico C Besta, Milan, Italy.
J Neurol Neurosurg Psychiatry. 1992 Nov;55(11):1027-31. doi: 10.1136/jnnp.55.11.1027.
To evaluate conduction along the proximal and distal segments of motor and sensory long limb nerves, as well as along the very short acoustic nerve, F response and somatosensory and brainstem auditory evoked potential were studied in a series of patients with hereditary motor and sensory neuropathy (HMSN) types I and II. A diffuse and comparable slowing of conduction in proximal and distal nerve segments, as well as along the acoustic nerve, seems to favour a primary myelin defect in HMSN I. F response and motor conduction velocity showed a similar derangement in both proximal and distal motor segments. Latencies of somatosensory evoked potentials were symmetrically prolonged and correlated with motor nerve impairment. Central conduction times were normal. Studies of brainstem auditory evoked potentials showed a high incidence of acoustic nerve involvement, the most evident abnormality being a statistically significant increase in the latency of the I wave. Our data seem to support the presence of primary myelinopathic damage in HMSN I.
为评估运动和感觉性长肢神经近端和远端节段以及极短的听神经的传导情况,对一系列I型和II型遗传性运动和感觉神经病(HMSN)患者进行了F波反应、体感诱发电位和脑干听觉诱发电位研究。近端和远端神经节段以及听神经的弥漫性且相当程度的传导减慢似乎支持HMSN I型存在原发性髓鞘缺陷。F波反应和运动传导速度在近端和远端运动节段均表现出类似的紊乱。体感诱发电位的潜伏期对称延长,并与运动神经损伤相关。中枢传导时间正常。脑干听觉诱发电位研究显示听神经受累发生率高,最明显的异常是I波潜伏期有统计学意义的增加。我们的数据似乎支持HMSN I型存在原发性髓鞘病变损害。