“…Studies in human patients with FM suggest that changes in the biochemical microenvironment of the facial nerve by processes such as demyelination, radiation, toxic effects, ischaemia hypoxia or oedema can induce axonal membrane hyperexcitability, resulting in spontaneous generation of myokymic and neuromyotonic discharges by mechanisms such as ectopic excitation, ephaptic excitation (cross‐talk) or autoexcitation 1,3 . This concept explains well the unilateral FM seen in human patients with disorders directly affecting either intra‐axial components of the facial nerve, such as in multiple sclerosis, 6 or extra‐axial components of the facial nerve, such as in Bell's palsy, 8 Guillain‐Barré syndrome, 1,23 cases of antibodies to voltage‐gated potassium channels, 12 and acoustic neuromas 17 or cholesteatomas involving the internal acoustic meatus 8 …”