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...

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Vydáno v:Neuromuscul Disord
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: 2015
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Article
On-line přístup: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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