Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases

Abstract
The previously unrecognised association of myoclonus in two patients with LHON with the 11778/ND4 pathogenic mutation is described. EEG failed to disclose epileptic figures, and a back averaging study suggested that myoclonus was cortical in origin in both patients.

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