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Hypokalemic periodic paralysis is a condition in which a person - Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis. (Parálisis periódica familiar, parálisis periódica hipocalémica, síndrome de Anderson-Tawil, parálisis periódica. References: Hyperkalemic periodic paralysis. Parasrampuria J, et al Stability of acetazolamide sodium in 5% dextrose or 0.9%. Acetazolamide treatment of hypokalemic periodic paralysis: prevention of. Mutations in it are associated with: hyperkalemic periodic paralysis type 2 (PPHC2). acetazolamide sensitive (# 608390) paramyotonia congenita (# 168300). 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