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Up to: Hereditary skeletal muscle disorder · Myotonic syndrome · SCN4A-related channelopathy
Potassium-aggravated myotonia
Potassium-aggravated myotonia (PAM) is a muscular channelopathy presenting with a pure myotonia dramatically aggravated by potassium ingestion, with variable cold sensitivity and no episodic weakness. This group includes three forms: myotonia fluctuans, myotonia permanens, and acetazolamide-responsive myotonia.
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Acetazolamide-responsive myotonia 0 trials
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Myotonia fluctuans 0 trials
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Myotonia permanens 0 trials