Trudell R G, Kaiser K K, Griggs R C
Neurology. 1987 Mar;37(3):488-91. doi: 10.1212/wnl.37.3.488.
We have studied 14 patients from a kindred with an autosomal dominant form of myotonia, with features differing from most cases of autosomal dominant or recessive myotonia congenita. All patients had painful muscle stiffness that was provoked by fasting and oral potassium administration and was relieved by carbohydrate-containing foods. Muscle biopsies showed the presence of type 1, 2A, and 2B fibers, as opposed to the absence of type 2B fibers seen in some patients with myotonia congenita. Acetazolamide was dramatically effective in alleviating myotonia in all patients and was more effective than other antimyotonic agents.
我们研究了一个患有常染色体显性遗传性肌强直的家族中的14名患者,其特征与大多数常染色体显性或隐性先天性肌强直病例不同。所有患者均有因禁食和口服钾诱发的疼痛性肌肉僵硬,食用含碳水化合物的食物后可缓解。肌肉活检显示存在1型、2A型和2B型纤维,这与一些先天性肌强直患者中不存在2B型纤维的情况相反。乙酰唑胺对所有患者的肌强直缓解均有显著效果,且比其他抗肌强直药物更有效。