Peyronnard J M, Lapointe L, Bouchard J P, Lamontagne A, Lemieux B, Barbeau A
Can J Neurol Sci. 1976 Nov;3(4):313-7. doi: 10.1017/s0317167100025518.
Twenty-six of 50 patients were investigated with nerve conduction studies and electromyography using a standard protocol and were compared to the findings in 50 normal control subjects. Almost all cases of typical Friedreich's ataxia had absent sensory action potentials (SAP) in the digital (92%) or sural (96%) nerves. The others had markedly decreased S.A.P's. In these same patients motor conduction velocities were either normal or only slightly decreased. In the second, atypical group of 9 patients, the motor conduction velocities were considerably decreased. Because of the absence of sensory action potentials in Friedreich's ataxia, and that the absence was noted in our very mild cases, it is proposed that this measure be used to facilitate early diagnosis.
50名患者中的26名按照标准方案接受了神经传导研究和肌电图检查,并与50名正常对照者的检查结果进行了比较。几乎所有典型弗里德赖希共济失调病例的指神经(92%)或腓肠神经(96%)感觉动作电位(SAP)均缺失。其他患者的SAP明显降低。在这些相同患者中,运动传导速度正常或仅略有降低。在第二组9名非典型患者中,运动传导速度明显降低。由于弗里德赖希共济失调患者存在感觉动作电位缺失,且在我们的极轻症病例中也观察到了这种缺失,因此建议采用该指标以促进早期诊断。