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Neuromuscul Disord ; 30(5): 424-426, 2020 05.
Article in English | MEDLINE | ID: mdl-32327288

ABSTRACT

Nav1.4 channelopathies due to SCN4A mutations can present with episodic attacks of myotonia triggered by fluctuation in the potassium level (potassium-aggravated myotonia). We report a case of potassium-aggravated myotonia due to Nav1.4-M1592V channelopathy with severe and long-lasting focal attacks of myotonia resembling dystonic posturing with diffuse muscle edema in the affected muscles in magnetic resonance imaging and almost constant presence of myotonic discharges in electromyography that can best be described as focal "status myotonicus".


Subject(s)
Channelopathies/complications , Channelopathies/genetics , Myotonia/diagnosis , Myotonia/etiology , NAV1.4 Voltage-Gated Sodium Channel/genetics , Adult , Electromyography , Female , Humans , Magnetic Resonance Imaging
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