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Hyperkalemic periodic paralysis type 1 (hyperPP1) is characterized by attacks of flaccid limb weakness. ABSTRACT Hypokalemic periodic paralysis is a rare congenital disease. Acetazolamide treatment of hypokalemic paralysis. Engel WK. La parálisis periódica hiperpotasémica puede ocurrir con miotonía o paramiotonía, y a. Hyperkalemic periodic paralysis and the adult muscle sodium channel. Sodium channel mutations in acetazolamide-responsive myotonia congenita. a) Parálisis periódica hiperkaliémica (PPHiperK). (AD –17q23.1q25–. Myotonia. Paramyotonia. Periodic paralysis. Paramyotonia congenital or hyperkalemic periodic paralisis? Clinical. genita with acetazolamide. Can J Neurol Sci. Publication » Acetazolamide Treatment of Hypokalemic Periodic Paralysis. 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