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Hyperkalemic periodic paralysis (hyperKPP) and paramyotonia congenita(PC) are genetic muscle disorders sharing the common features of myotonia and. Thyrotoxic periodic paralysis and encephalopathy as presenting symptoms of. recessive myotonia congenita responsive to acetazolamide. Arch Neurol. 1975 Jun;32(6):385-92. Acetazolamide treatment of hypokalemic periodic paralysis. Probable mechanism of action. Vroom FW, Jarrell MA, Maren. Managing Periodic Paralysis 101. Hypokalemic Periodic Paralysis. • Identifying Triggers. Diamox. (Acetazolamide). – Dose: 62.5 – • Daranide. acetazolamide. Investig Med 50:125-132, 2002. Severe Prognosis in a Large Family with Hypokalemic Periodic Paralysis. Muscle Nerve 27:165-169, 2003. arimidex dopo 5 anni new/6091-1-11581.php L' acetazolamide è un principio attivo che fa parte della classe degli. 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