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Effects of acetazolamide on overnight oxygenation and acute mountain. Report of three cases treated with paralysis and controlled respiration. new/7189-1-9130.php The periodic hyperpotassemia paralysis is a striated muscle channelopathy. episodes of muscular asthenia at 2 months of treatment onset with oral acetazolamide. and phenotype associated with familial hyperkalemic periodic paralysis. Defects in SCN4A are the cause of hyperkalemic periodic paralysis (HYPP). fluctuans, severe myotonia permanens, and acetazolamide-responsive myotonia. La parálisis periódica es una rara condición heredada que causa episodios ocasionales de debilidad muscular severa. Hyperkalemic periodic paralysis. (Parálisis periódica familiar, parálisis periódica hipocalémica, síndrome de Anderson-Tawil, parálisis periódica. 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