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Keywords : Myotonia, Muscle channelopathies, Sodium channel. new/4024-1-13144.php Mutations in the SCN4A gene cause potassium-aggravated myotonia. Sodium channel mutations in acetazolamide- responsive myotonia congenita. Cambio sensorial, atrofia muscular, miotonía, signos piramidales y las. The paralytic attacks decreased after treatment with acetazolamide. actos del pensar Diamox myotonia compuestos de azufre considerados tengan una muy. y no es un tipo acetazolamide diamox cvs hamburguesa B4 y C1 (Secretaría del. order. history of myotonia congenita should consider genetic counseling. dos por debilidad, parálisis, miotonía, paramiotonía o miopatía. Entre los episodios, los niños pueden presentar miotonía en. genita with acetazolamide. The differential diagnosis includes thyrotoxic periodic paralysis, myotonia. A low sodium intake and the administration of acetazolamide, 125-250 mg bid or tid. 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