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Molecular diagnosis of hyperkalemic periodic paralysis (SCN4A gene); Genetica AG. Molecular diagnosis of Acetazolamide-Responsive Congenital Myotonia. responsive to acetazolamide (AZM). Hyperkalemic periodic paralysis type 1 (hyperPP1) is characterized by attacks of flaccid limb weakness. tornos del músculo: la parálisis periódica con o sin cambios del potasio,miastenia o desordenes miastenicos. Alteration of Ca channels cause muscle dysfunction periodic paralysis with or without. tion in acetazolamide-responsive myotonia congenita, pa- ramyotonia congenita and hyperkalemic periodic paralysis. new/5963-1-9069.phpnew/4654-1-3682.php Diamox comprimidos y cápsulas e inyección Diamox SR todos. 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