Neurological channelopathies: classification
Written and reviewed by Dr Ibrahim Imam, Consultant Neurologist. Last reviewed .
Neurological channelopathies: classification. Hyperkalaemic periodic paralysis, Hypokalaemic periodic paralysis. Fully referenced neurology checklist.
Muscle channelopathies: periodic paralyses
- Hyperkalaemic periodic paralysis
- Hypokalaemic periodic paralysis
Muscle channelopathies: non-dystrophic myotonias
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Muscle channelopathies: ryanodinopathies
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Epileptic channelopathies
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Pain syndromes
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Ataxic syndromes
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Other channelopathy syndromes
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References
- Rakowicz W, Hanna M. Muscle ion channel diseases. ACNR 2003; 3:14-16.
- Platt D, Griggs R. Skeletal muscle channelopathies: new insights into the periodic paralyses and nondystrophic myotonias. Curr Opin Neurol 2009; 22:524-531.
- Horga A, Raja Rayan DL, Matthews E, et al. Prevalence study of genetically defined skeletal muscle channelopathies in England. Neurology 2013; 80:1472-1475.
- Spillane J, Kullmann DM, Hanna MG. Genetic neurological channelopathies: molecular genetics and clinical phenotypes. JNNP 2016; 87:37-48.
- Kullmann DM, Waxman SG. Neurological channelopathies: new insights into disease mechanisms and ion channel function. J Physiol 2010; 588:1823-1827.
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