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Hypokalemic periodic paralysis is a rare congenital disease. It's characterized by a. Hypokalemic periodic paralysis presents in 1 of each 100,000; in addition it affects more frequently males than. Acetazolamide treatment of hypokalemic. Periodic Paralysis: Safety Comparison of #Keveyis (dichlorphenamide) vs. #Diamox (acetazolamide) (dichlorphenamide) for Primary Hyperkalemic and Hypokalemic Periodic Paralysis - SUBSTRACTION ACETAZOLAMIDE SPECT CO-REGISTERED TO. Artigo: SUCCESSFUL TREATMENT OF HYPOKALEMIC PERIODIC PARALYSIS. Molecular diagnosis of hypokalemic periodic paralysis (SCN4A gene); Genetica AG. Molecular diagnosis of Acetazolamide-Responsive Congenital Myotonia. Dihydropiridine receptor mutations cause hypokalemic periodic paralysis. Cell 1994; 77: 8638. 16. 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