The previously unrecognised association of myoclonus in two patients with LHON with the 11778/ND4 pathogenic mutationis described. EEG failed to disclose epileptic figures, and a back averaging study suggested that myoclonus was cortical inorigin in both patients.
Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases / V., Carelli; M. L., Valentino; R., Liguori; Meletti, Stefano; R., Vetrugno; F., Provini; G. L., Mancardi; F., Bandini; A., Baruzzi; P., Montagna. - In: JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY. - ISSN 0022-3050. - STAMPA. - 71:6(2001), pp. 813-816. [10.1136/jnnp.71.6.813]
Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases
MELETTI, Stefano;
2001
Abstract
The previously unrecognised association of myoclonus in two patients with LHON with the 11778/ND4 pathogenic mutationis described. EEG failed to disclose epileptic figures, and a back averaging study suggested that myoclonus was cortical inorigin in both patients.
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