Persistent facial myokymia associated with K(+) channel antibodies
Related Experiment Video
Updated: Oct 3, 2026

Isolation and Kv Channel Recordings in Murine Atrial and Ventricular Cardiomyocytes
Published on: March 12, 2013
L Gutmann1, J G Tellers, S Vernino
1Department of Neurology, West Virginia University, Morgantown 26506, USA. lgutmann@wvu.edu
Abstract:
A 58-year-old woman developed bilateral facial myokymia in 1978, persisting for the next 23 years and associated with high titers of voltage-gated K(+) channel (VGKC) antibodies. Brain imaging failed to show a pontine lesion. The clinical facial myokymia and electromyographic doublets and multiplets (43 to 250 Hz) were milder and more restricted than those seen in generalized neuromyotonic disorders with VGKC antibodies. This case and another reported recently represent a focal VGKC antibody syndrome.
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