Persistent facial myokymia associated with K+ channel antibodies

Ludwig Gutmann, John G. Tellers, Steven Vernino

Research output: Contribution to journalArticle

17 Citations (Scopus)

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.

Original languageEnglish (US)
Pages (from-to)1707-1708
Number of pages2
JournalNeurology
Volume57
Issue number9
StatePublished - Nov 13 2001

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Facial Nerve Diseases
Voltage-Gated Potassium Channels
Antibodies
Neuroimaging

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Persistent facial myokymia associated with K+ channel antibodies. / Gutmann, Ludwig; Tellers, John G.; Vernino, Steven.

In: Neurology, Vol. 57, No. 9, 13.11.2001, p. 1707-1708.

Research output: Contribution to journalArticle

Gutmann, L, Tellers, JG & Vernino, S 2001, 'Persistent facial myokymia associated with K+ channel antibodies', Neurology, vol. 57, no. 9, pp. 1707-1708.
Gutmann, Ludwig ; Tellers, John G. ; Vernino, Steven. / Persistent facial myokymia associated with K+ channel antibodies. In: Neurology. 2001 ; Vol. 57, No. 9. pp. 1707-1708.
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