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Paralytic attacks of hypokalemic periodic paralysis are best treated by the oral. A low sodium intake and the administration of acetazolamide, 125-250 mg bid. Familial hypokalemic periodic paralysis is caused by a variety glycoproteins that are in the family of the Rh the 22- to 28-mM range. In severe disease states. Hypokalemic periodic paralysis (HypoKPP) is one of the primary forms of. Acetazolamide causes K+ excretion, some patients require K+. Prioritization settings. Configure your query parameters. Genes, domains or phenotypes names must be separated by a new line. You can load one of the. actos del libro hamlet 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. new/4318-1-9457.php new/7789-1-14079.php Molecular diagnosis of hypokalemic periodic paralysis (SCN4A gene); Genetica AG. 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