Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases
Open Access
- 1 December 2001
- journal article
- case report
- Published by BMJ in Journal of Neurology, Neurosurgery & Psychiatry
- Vol. 71 (6) , 813-816
- https://doi.org/10.1136/jnnp.71.6.813
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.Keywords
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