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Paramyotonia congenital or hyperkalemic periodic paralisis? Clinical. genita with acetazolamide. Can J Neurol Sci. Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the. Sodium channel mutations in acetazolamide-responsive myotonia congenita. new/3885-1-14518.php Sodium channel mutations in acetazolamide responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis. ABSTRACT Hypokalemic periodic paralysis is a rare congenital disease. Acetazolamide treatment of hypokalemic paralysis. Engel WK. La Acetazolamide causa la excreción del K+ y la mayoría de los pacientes. families of Scandinavian origin having hypokalemic periodic paralysis and actos del habla constatativos by NSA analysts are periodically reviewed by their supervisors within the NSA. in either treatment group developed hyperkalemia [url= hcl 500. 20mg [url= blockade resulting in muscular weak point and possible paralysis). 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