Abstract
Ion channelopathies have common clinical features, recurrent patterns of mutations, and almost predictable mechanisms of pathogenesis. In skeletal muscle, disorders are associated with mutations in voltage-gated Na(+), K(+), Ca(2+), and Cl(-) channels leading to hypoexcitability, causing periodic paralysis and to hyperexcitabilty, resulting in myotonia or susceptibility to malignant hyperthermia.
MeSH terms
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Humans
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Ion Channels / genetics
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Ion Channels / metabolism*
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Malignant Hyperthermia / genetics
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Malignant Hyperthermia / metabolism
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Malignant Hyperthermia / physiopathology
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Muscle, Skeletal / innervation
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Muscle, Skeletal / metabolism*
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Muscle, Skeletal / physiopathology
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Muscular Diseases / genetics
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Muscular Diseases / metabolism*
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Muscular Diseases / physiopathology
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Mutation / genetics
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Myotonia / genetics
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Myotonia / metabolism
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Myotonia / physiopathology
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Paralysis, Hyperkalemic Periodic / genetics
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Paralysis, Hyperkalemic Periodic / metabolism
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Paralysis, Hyperkalemic Periodic / physiopathology
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Sarcolemma / genetics
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Sarcolemma / metabolism*