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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Neuromuscul Disord
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2015
Pynciau:
Article
Mynediad Ar-lein: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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