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Divalent cation-responsive myotonia and muscle paralysis in skeletal muscle sodium channelopathy

We report a patient with paramyotonia congenita/hyperkalemic periodic paralysis due to Nav1.4 I693T mutation who had worsening of myotonia and muscle weakness in the setting of hypomagnesemia and hypocalcemia with marked recovery after magnesium administration. Computer simulations of the effects of...

詳細記述

保存先:
書誌詳細
出版年:Neuromuscul Disord
主要な著者: Mankodi, Ami, Grunseich, Christopher, Skov, Martin, Cook, Lisa, Aue, Georg, Purev, Enkhtsetseg, Bakar, Dara, Lehky, Tanya, Jurkat-Rott, Karin, Pedersen, Thomas H, Childs, Richard W
フォーマット: Artigo
言語:Inglês
出版事項: 2015
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4630112/
https://ncbi.nlm.nih.gov/pubmed/26494408
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nmd.2015.08.007
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