This review elucidates how sodium channel mutations disrupt inactivation to cause the excitability derangements seen in myotonia and periodic paralysis.
Informs diagnosis of channelopathies; extends mechanistic models but leaves targeted therapies open.
Myotonias and periodic paralyses constitute a diverse group of inherited disorders of muscle in which the primary defect is an alteration in the electrical excitability of the muscle fiber. The ion channel defects underlying these excitability derangements have recently been elucidated at the molecular and functional levels. This review focuses on sodium channel mutations that disrupt inactivation and thereby cause both the enhanced excitability of myotonia (muscle stiffness due to repetitive discharges) and the inexcitability resulting from depolarization during attacks of paralysis.
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Stephen C. Cannon (1996) studied this question.
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