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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. Publication » Acetazolamide Treatment of Hypokalemic Periodic Paralysis. ACETAZOLAMIDE-RESPONSIVE » HEREDITARY. PAROXYSMAL CEREBELLAR. HYPOKALEMIC PERIODIC PARALYSIS, HOKPP. 170400. CACNA1S. Thyrotoxic Periodic Paralysis (TPP) is a potentially lethal manifestation of hyperthyroidism which is. Acetazolamide has no role in the treatment of TPP. tirotóxica: Caso clínico Thyrotoxic hypokalemic periodic paralysis: Report of one case actos de habla locutivo perlocutivo Palabras clave: parálisis periódica familiar, hipopotasemia. Hypokalemic periodic paralysis is a rare congenital disease. Acetazolamide treatment. 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