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Up to: Hereditary neuromuscular disease · Muscular channelopathy

SCN4A-related channelopathy

Any muscular channelopathy in which the cause of the disease is a variation in the SCN4 gene. This is characteristic of a continuum in the clinical spectrum that includes sodium-channel myotonia, paramyotonia congenita, hypokalemic periodic paralysis type II and hyperkalemic periodic paralysis.

1 trial tagged with this condition →

Hyperkalemic periodic paralysis 1 trial
Paramyotonia congenita of Von Eulenburg 1 trial
Hypokalemic periodic paralysis, type 2 0 trials
Potassium-aggravated myotonia 0 trials Sub-types →