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Myotonic disorders: A review article

机译:肌强直性疾病:评论文章

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摘要

The myotonic disorders are a heterogeneous group of genetically determined diseases that are unified by the presence of myotonia, which is defined as failure of muscle relaxation after activation. The presentation of these disorders can range from asymptomatic electrical myotonia, as seen in some forms of myotonia congenita (MC), to severe disability with muscle weakness, cardiac conduction defects, and other systemic features as in myotonic dystrophy type I (DM1). In this review, we describe the clinical features and pathophysiology of the different myotonic disorders, their laboratory and electrophysiologic findings and briefly review the currently available treatments.
机译:肌强直性疾病是由遗传决定的疾病的异质性组,其通过肌强直的存在而统一,肌强直被定义为激活后肌肉松弛的失败。这些疾病的表现范围从无症状性先天性肌强直(MC)所见到的无症状性肌强直到严重的残疾,包括肌肉无力,心脏传导缺陷和其他系统性特征,如I型强直性营养不良(DM1)。在这篇综述中,我们描述了不同肌强直性疾病的临床特征和病理生理学,它们的实验室和电生理学发现,并简要回顾了当前可用的治疗方法。

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