Alterations in this channel produce flaccid paralysis, arrhythmias, impaired skeletal. correlation and therapeutic rationale in hyperkalemic periodic paralysis. Amiodarone and acetazolamide for the treatment of genetically. ABSTRACT Hypokalemic periodic paralysis is a rare congenital disease. Acetazolamide treatment of hypokalemic paralysis. Engel WK. This data show the remarkable benefit of acetazolamide on permanent weakness of hyperkalemic periodic paralysis in association with the T704M mutation. (ACETAB) ACETAZOLAMIDE is marketed in ( VENEZUELA ) can. Hypokalemic periodic paralysis is a condition in which a person has. Palabras clave: parálisis periódica familiar, hipopotasemia. Hypokalemic periodic paralysis is a rare congenital disease. Acetazolamide treatment. Neurología 2008;23(7):427-435. Hyperkalemic periodic paralysis: a Spanish. Sodium channel mutations in acetazolamide-responsive myotonia congenital. 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