Subramony S H, Malhotra C P, Mishra S K
Muscle Nerve. 1983 Jun;6(5):374-9. doi: 10.1002/mus.880060506.
Compound muscle action potential (CMAP) amplitudes, response to 2 Hz nerve stimulation, response to exercise and electromyographic needle electrode examination findings from the thenar muscles of two patients with paramyotonia congenita were compared with those from two patients with dominantly inherited myotonia congenita in warm (34 degrees C) and cold (20 degrees C) states. Cold induced a significant fall in CMAP amplitude, induced/worsened a significant decremental response to 2 Hz stimulation, and virtually abolished myotonia and voluntary recruitment of motor unit potentials in patients with paramyotonia congenita; none of these occurred in myotonia congenita. Though exercise induced a mild fall in CMAP amplitude in both groups, postexercise fibrillations occurred only in patients with paramyotonia congenita. These findings serve to distinguish these two entities in the clinical electromyography laboratory.
将两名先天性副肌强直患者和两名常染色体显性遗传先天性肌强直患者在温暖(34摄氏度)和寒冷(20摄氏度)状态下的复合肌肉动作电位(CMAP)振幅、对2赫兹神经刺激的反应、对运动的反应以及拇短展肌的肌电图针电极检查结果进行了比较。寒冷导致先天性副肌强直患者的CMAP振幅显著下降,诱发/加重了对2赫兹刺激的显著递减反应,并且几乎消除了肌强直和运动单位电位的自主募集;而先天性肌强直患者未出现上述任何情况。尽管运动在两组中均导致CMAP振幅轻度下降,但运动后纤颤仅发生在先天性副肌强直患者中。这些发现有助于在临床肌电图实验室中区分这两种疾病。