myotonic disorders: a review article

Authors

chris hahn department of neurology, brigham and women’s hospital, harvard medical school, ‎boston, usa

mohammad kian salajegheh department of neurology, brigham and women’s hospital, harvard medical school, ‎boston, usa

abstract

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.

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Journal title:
iranian journal of neurology

جلد ۱۵، شماره ۱، صفحات ۴۶-۵۳

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