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Article

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

Journal of neurology, neurosurgery, and psychiatry - 1 Dec 2001

Carelli V, Valentino M L, Liguori R, Meletti S, Vetrugno R, Provini F, Mancardi G L, Bandini F, Baruzzi A, Montagna P

Abstract excerpt

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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Source

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Identifiers

PMID: 11723211
DOI: 10.1136/jnnp.71.6.813
PMCID: PMC1737658

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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