characterized by acetazolamide-responsive attacks of cerebellar ataxia and. Dihydropyridine receptor mutations cause hypokalemic periodic paralysis. Things that Prevent Attacks Chronically: mexilitene, acetazolamide, phenytoin, quinine, carbamazepine. Hypokalemic Periodic Paralysis. actos de comercio objetivos en venezuela ABSTRACT Hypokalemic periodic paralysis is a rare congenital disease. Acetazolamide treatment of hypokalemic paralysis. Engel WK. Mutations in it are associated with: hyperkalemic periodic paralysis type 2 (PPHC2). acetazolamide sensitive (# 608390) paramyotonia congenita (# 168300). CACNA1S mutations are associated with hypokalemic periodic paralysis type 1. La Parálisis Periódica Hipocaliémica Familiar (PPHF) es una enfermedad. Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of. Med Int Mex 2008;24(1):69-75 Caso clínico Parálisis periódica familiar. 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