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Article

Leber's hereditary optic neuropathy with intracranial arteriovenous malformation: a case report.

Acta neurologica Belgica - 1 Jun 2002

Fujitake Junko, Mizuta Haruo, Fujii Hayato, Ishikawa Yasuhiro, Sasamoto Kenji, Goto Yu-ichi, Nonaka Ikuya, Tatsuoka Yoshihisa

Abstract excerpt

We reported a patient with Leber's hereditary optic neuropathy (LHON) with an intracranial arteriovenous malformation (AVM). Genetic analysis of this patient revealed a point mutation in mitochondrial DNA (mtDNA) at nucleotide position 11,778 in the ND4 subunit of complex I. Although the relationship between intracranial AVM and mtDNA mutations remains uncertain, some patients with intracranial AVM may be...

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Source

Identifiers

PMID: 12161905

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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