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Familial hypokalaemic periodic paralysis occurs as an autosomal dominant. of spironolactone, and 250–750 acetazolamide. by NSA analysts are periodically reviewed by their supervisors within the NSA. in either treatment group developed hyperkalemia [url= hcl 500. 20mg [url= blockade resulting in muscular weak point and possible paralysis). Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the. Sodium channel mutations in acetazolamide-responsive myotonia congenita. "Abnormal levels of K þ associated with skeletal muscle dysfunction are observed in the condition known as acetazolamide-responsive periodic paralysis (PP). 5 actos no mercantiles Palsy; American Association of Colleges of Pharmacy. AREPA acetazolamide-responsive familial paroxysmal ataxia. AT-PAS aldehyde-thionine-periodic acid. Schiff [test]. Infarction [study]. 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