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Familial hypokalaemic periodic paralysis occurs as an autosomal dominant. 100–200 of spironolactone, and 250–750 acetazolamide. new/8453-1-17615.php Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype. Matthews E. MRCP. 1., Portaro S. M.D. 1,2., Ke Q. M.D. 3,5. actos de comunicación en el proceso civil Med Int Mex 2008;24(1):69-75 Caso clínico Parálisis periódica familiar. Hypokalemic periodic paralysis presents in 1 of each 100,000; in addition it affects more. Acetazolamide treatment of hypokalemic paralysis. 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