Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Leber hereditary optic neuropathy, progressive visual loss, and multiple-sclerosis-like symptoms.

American journal of ophthalmology - 1 Oct 2001

Tran M, Bhargava R, MacDonald I M

Abstract excerpt

PURPOSE: To report a case of Leber hereditary optic neuropathy with multiple-sclerosis-like symptoms. METHODS: Observational case report. A 34-year-old man was found to have Leber hereditary optic neuropathy and a mutation at position 11778 of the mitochondrial genome. The progression of vision loss and onset of weakness in the right leg warranted neuroimaging. RESULTS: Magnetic resonance imaging documented...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Optic Atrophies, Hereditary
Share to Disease Progression
Share to DNA, Mitochondrial

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Magnetic Resonance Imaging

Share to Mitochondria

Share to Multiple Sclerosis

Share to Mutation

Share to Vision Disorders

Source

Identifiers

PMID: 11589893
DOI: 10.1016/s0002-9394(01)01045-5

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Leber hereditary optic neuropathy, progressive visual loss, and multiple-sclerosis-like symptoms.PMID 11589893Read ↗

Leber’s hereditary optic neuropathy and multiple sclerosis: overlap between mitochondrial disease and neuroinflammationSemantic proximity Read ↗

Leber hereditary optic neuropathySemantic proximity Read ↗

Mitochondrial Mutations in Multiple Sclerosis Patients with Atypical Optic Neuropathy.Semantic proximity Read ↗

Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man.Semantic proximity Read ↗

Leber's hereditary optic neuropathy associated with multiple sclerosis: Harding's syndrome.Semantic proximity Read ↗

Leber hereditary optic neuropathy.Semantic proximity Read ↗

[Leber's hereditary optic neuropathy].Semantic proximity Read ↗

Late-onset Leber's hereditary optic neuropathy presenting with longitudinally extensive myelitis harbouring the m.14484T>C mutation: Extending the genotype-phenotype spectrum.Semantic proximity Read ↗

Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutations.Semantic proximity Read ↗

Leber’s hereditary optic neuropathy is multiorgan not mono-organSemantic proximity Read ↗

Clinical features of Leber's hereditary optic neuropathy with the 11778 mitochondrial DNA mutation in Taiwanese patients.Semantic proximity Read ↗

Leber's optic neuropathy associated with disseminated white matter disease: a case report and review.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.