Abstract
Treatment of paramyotonia congenita with acetazolamide has been shown to reduce myotonic symptoms but severe weakness has developed in some patients leading to a recommendation not to use the drug in this disorder. We studied a patient with the characteristic clinical and electrophysiological profile of paramyotonia congenita. Myotonia was effectively treated with a very low dose of acetazolamide and no weakness developed. We conclude that acetazolamide can be a safe and effective medication in paramyotonia congenita. © 1987, Canadian Neurological Sciences Federation. All rights reserved.
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CITATION STYLE
Benstead, T. J., Camfield, P. R., & King, D. B. (1987). Treatment of Paramyotonia Congenita with Acetazolamide. Canadian Journal of Neurological Sciences / Journal Canadien Des Sciences Neurologiques, 14(2), 156–158. https://doi.org/10.1017/S0317167100026305
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