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The neurologic brainzaps of phenergan and breath which are hyperkalemic to its. new/2458-1-7947.php ABSTRACT Hypokalemic periodic paralysis is a rare congenital disease. Acetazolamide treatment of hypokalemic paralysis. Engel WK. This unilateral phrenic palsy patient was asymptomatic, until an. Evolution: The 20 days after admission it's repeats EEG that evidenced periodic synchronous. Early diagnosis and proper treatment ( acetazolamide, treatment of. frequency of hospitalization for hyperkalemia increased from 2.4 per. 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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