Describes familial hyperkalemic paralysis with myotonia, a condition where potassium administration precipitates rather than relieves attacks of weakness.
May worsen attacks with potassium in familial myotonic paralysis; leaves open genetic mechanisms and management strategies.
ALTHOUGH it has long been known that a striking fall in serum potassium level may coincide with the attacks of weakness occurring in familial periodic paralysis, and that the administration of potassium salts may relieve such an attack,1 2 3 other families suffering from similar attacks have been described in which no such change in potassium level or relief followed potassium administration.4 , 5 In 1956 Gamstorp6 described in detail 17 cases from two families suffering from periodic weakness with normal or slightly elevated serum potassium levels during attacks and a striking response to orally administered potassium chloride, which, instead of relieving an attack, . . .
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Meulen et al. (1961) studied this question.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: