Claus D, Schöcklmann H O, Dietrich H J
Eur Arch Psychiatry Neurol Sci. 1986;235(6):355-60. doi: 10.1007/BF00381004.
Long latency reflexes were measured from the hand muscles of 27 patients suffering from different cerebellar diseases (12 diffuse cerebellar atrophies, 7 cerebellar hemispheric infarcts, 8 Friedreich's disease) and from 45 controls after electrical stimulus of the median nerve at the wrist. The M3 response (latency about 70 ms) was increased in about 50% of cerebellar atrophy cases and occasionally (10 of 12 cases) separated from the M2 response (50 ms). M3 was sometimes (3/7) increased and the M2-3 complex was prolonged ipsilaterally in cases of cerebellar infarcts. In the cases of Friedreich's ataxia M2 was always lost uni or bilaterally because of the disturbance of afferent or efferent fibres. The latencies of the spinal reflex M1 and also of M2 were not always increased strongly enough to be clearly separated from the normal values.
对27例患有不同小脑疾病的患者(12例弥漫性小脑萎缩、7例小脑半球梗死、8例弗里德赖希共济失调)以及45名对照者的手部肌肉进行正中神经腕部电刺激后测量长潜伏期反射。在约50%的小脑萎缩病例中,M3反应(潜伏期约70ms)增强,且在12例中有10例偶尔与M2反应(50ms)分离。在小脑梗死病例中,M3有时(3/7)增强,同侧M2 - 3复合波延长。在弗里德赖希共济失调病例中,由于传入或传出纤维的紊乱,M2总是单侧或双侧消失。脊髓反射M1以及M2的潜伏期并非总是增强到足以与正常值明显区分开来。