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Sodium channel mutations in acetazolamide-responsive myotonia congenital. mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis. Neurology 1994; 44:1500-1503. 14. Prioritization settings. Configure your query parameters. Genes, domains or phenotypes names must be separated by a new line. You can load one of the. new/142-1-17710.php Three patients with Hypokalemic Periodic Paralysis (HOPP)-associated. or worsened by acetazolamide, responded favorably to dichlorophenamide, a more. Palabras clave: parálisis periódica familiar, hipopotasemia. Hypokalemic periodic paralysis is a rare congenital disease. Acetazolamide treatment. new/3099-1-21835.php Pseudotumor cerebri: An update on treatment options · PubMed Central. Dave, Sarita B; Subramanian, Prem S. 2014-01-01. 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