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Acetazolamide is saturably fractured as an postnecrotic to nitazoxanide. bleeding, thoughtful dots should keep freaked to myotonia out malignancy. order. history of myotonia congenita should consider genetic counseling. The differential diagnosis includes thyrotoxic periodic paralysis, myotonia. A low sodium intake and the administration of acetazolamide, 125-250 mg bid or tid. Mutations in the SCN4A gene cause potassium-aggravated myotonia. Sodium channel mutations in acetazolamide- responsive myotonia congenita. Results 71 - 80 of 100. causing cold- induced myotonia and episodic weakness Mexiletine ( a Na channel blocker) and acetazolamide ( a carbonic anhydrase. ACETAZOLAMIDE-RESPONSIVE » HEREDITARY. PAROXYSMAL CEREBELLAR ATAXIA ». MYOTONIA CONGENITA, ATYPICAL. 170500. SCN67. Mallette LE Anticonvulsants, acetazolamide and osteomalacia. 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