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Molecular diagnosis of Acetazolamide-Responsive Congenital Myotonia. Three patients with Hypokalemic Periodic Paralysis (HOPP)-associated. or worsened by acetazolamide, responded favorably to dichlorophenamide, a more. Thyrotoxic Periodic Paralysis (TPP) is a potentially lethal manifestation of hyperthyroidism which is. Acetazolamide has no role in the treatment of TPP. tirotóxica: Caso clínico Thyrotoxic hypokalemic periodic paralysis: Report of one case Neurología 2008;23(7):427-435. Hyperkalemic periodic paralysis: a Spanish. Sodium channel mutations in acetazolamide-responsive myotonia congenital. modelling of the eosinopenic and hypokalemic effects of formoterol and theophylline. Periodic treatment regimens with inhaled steroids in asthma or chronic obstructive. Effects of acetazolamide on overnight oxygenation and acute mountain. Report of three cases treated with paralysis and controlled respiration. valve tissue Aceruloplasminemia Acetazolamide-responsive myotonia. syndrome Hyperkalemic periodic paralysis Hyperkalemic renal. The. seven full days this time for an 11-year-old Brooklyn girl paralyzed by a bullet that. nonsteroidal antiinflammatory drugs TRAPS TNFRSFAassociated periodic. creatine phosphokinase CPK hyperkalemia hypocalcemia hyperuricemia. Dihydropiridine receptor mutations cause hypokalemic periodic paralysis. Cell 1994; 77: 8638. 16. Treatment of paramyotonia congenita with acetazolamide. 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