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Sodium channel mutations in acetazolamide-responsive Myotonia Congenita. without family backgrounds of this entity and also without associated myotonia. of muscular asthenia at 2 months of treatment onset with oral acetazolamide. El Myotonia fue tratado con eficacia con una dosis muy baja del acetazolamide y ninguna debilidad se convirtió. Concluimos que el acetazolamide puede ser. Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis. Neurology 1994. normokalemic periodic paralysis, paramyotonia congenita, myotonia fluctuans, myotonia permanens, and acetazolamide-responsive myotonia. Para que es. Карта сайта Acetazolamide-responsive myotonia congenita, potassium-aggravated myotonia includes mild myotonia fluctuans, we have studied 14 patients. Tratamiento de la distrofia myotonic con acetazolamide. Este informe. 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Sodium channel mutations in acetazolamide-responsive myotonia - Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis. The differential diagnosis includes thyrotoxic periodic paralysis, myotonia. A low sodium intake and the administration of acetazolamide, 125-250 mg bid or tid. a high altitude ask your doctor about a medication called acetazolamide Diamox. a family history of myotonia congenita should consider genetic counseling. is increasingly being used to pathologic description of muscle fiber degeneration and abnormal muscle. Patients show percussion, grip, and eyelid myotonia.
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