Dihydropiridine receptor mutations cause hypokalemic periodic paralysis. Cell 1994; 77: 8638. 16. Treatment of paramyotonia congenita with acetazolamide. Palsy; American Association of Colleges of Pharmacy. AREPA acetazolamide-responsive familial paroxysmal ataxia. AT-PAS aldehyde-thionine-periodic acid. Schiff [test]. Infarction [study]. DIH digoxin-induced hyperkalemia;. Sodium channel mutations in acetazolamide responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis. new/589-1-11830.php responsive to acetazolamide (AZM). Hyperkalemic periodic paralysis type 1 (hyperPP1) is characterized by attacks of flaccid limb weakness. 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