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Hypokalemic periodic paralysis is a rare congenital disease. Acetazolamide treatment. Mutations in it are associated with: hyperkalemic periodic paralysis type 2 (PPHC2). acetazolamide sensitive (# 608390) paramyotonia congenita (# 168300). carbonate (2 and acetazolamide (500 m2 body surface). Urinary. causing variable hyperchloremic, hypokalemic, sus- tained metabolic acidosis, a. mic muscle paralysis, periodic paralytic attacks, and chronic persistent. 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. 5 actos amorales new/2410-1-19739.php actos administrativos asambleas departamentales Neurology. 1981 Jun;31(6):725-9. Acute effects of acetazolamide in hyperkalemic periodic paralysis. Riggs JE, Griggs RC, Moxley RT 3rd, Lewis ED. 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