Evidence map›Paper›PMID 41847276›Full record

ArticleNeuro-ophthalmology (Aeolus Press)2026

Visual Loss from Leber's Optic Neuropathy Presenting in a 76-Year-Old Man with the 14484 Mutations.

Laura Goldfarb Cyrino, Bianca Jimena Saldaña Lagos, Pedro Henrique Varalta Martins, Julia F Bonato Cavalcanti, Leonardo E Ariello, Mario Luiz Ribeiro Monteiro

Abstract readCase Reports
In one paragraph

Article in Neuro-ophthalmology (Aeolus Press), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Laura Goldfarb CyrinoDivision of Ophthalmology, University of São Paulo Medical School, São Paulo, Brazil.ORCID https://orcid.org/0000-0001-6007-6662
Bianca Jimena Saldaña LagosMedical Student, University of São Paulo Medical School, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-2949-6690
Pedro Henrique Varalta MartinsMedical Student, University of São Paulo Medical School, São Paulo, Brazil.
Julia F Bonato CavalcantiDivision of Neurology, University of São Paulo Medical School, São Paulo, Brazil.
Leonardo E ArielloDivision of Ophthalmology, University of São Paulo Medical School, São Paulo, Brazil.
Mario Luiz Ribeiro MonteiroDivision of Ophthalmology, University of São Paulo Medical School, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-7281-2791

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leber's Hereditary Optic Neuropathy (LHON) is an important hereditary optic neuropathy that typically causes bilateral visual loss, predominantly in male patients. While it usually manifests in young adults, it can uncommonly present in older individuals without a family history, potentially leading to diagnostic confusion. The mechanisms underlying why some individuals with these mutations develop optic neuropathy while others remain asymptomatic are still under investigation. Factors such as heteroplasmy, epigenetic modifications, and environmental triggers, including alcohol consumption, are thought to contribute. However, the exact triggers that convert carriers into symptomatic individuals remain poorly understood, with cigarette smoking and alcohol intake being potential contributors. The purpose of this paper is to describe a 76-year-old patient who experienced, painless bilateral visual loss progressing over 4 weeks. Despite extensive evaluation, including imaging, blood tests, and genetic testing, a mitochondrial mutation (T14484C) associated with LHON was identified. Although LHON is rare, especially in the elderly, and usually presents in younger males, this case highlights the need for clinicians to consider LHON as a potential diagnosis in older patients presenting with unexplained visual loss.

Indexed as

ganglion cellsLeber’s hereditary optic neuropathymitochondrial mutationmtDNAoptic neuropathy

Identifiers

PMID41847276
PMCPMC12990940

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.