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...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
izdano v:Neuromuscul Disord
Main Authors: 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
Format: Artigo
Jezik:Inglês
Izdano: 2015
Teme:
Article
Online dostop: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
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki