Evidence map›Paper›PMID 41030890›Full record

ArticleBrain communications2025

Diagnosis and etiologic classification of optic tract lesions.

Natalie S Chen, Heather M McDonald, Jonathan Micieli, Edward Margolin

Abstract read
In one paragraph

Article in Brain communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers 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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Natalie S ChenTemerty Faculty of Medicine, University of Toronto, Toronto, Ontario M5S 3K3, Canada.ORCID https://orcid.org/0000-0003-4157-2710
Heather M McDonaldDepartment of Ophthalmology and Visual Sciences, University of Toronto, Toronto, Ontario M5T 3A9, Canada.
Jonathan MicieliDepartment of Ophthalmology and Visual Sciences, University of Toronto, Toronto, Ontario M5T 3A9, Canada.
Edward MargolinDepartment of Ophthalmology and Visual Sciences, University of Toronto, Toronto, Ontario M5T 3A9, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Existing literature regarding optic tract syndrome, which arises from lesions affecting the optic tract(s), is limited. The objective of this retrospective cohort study was to elucidate the diverse clinical and imaging manifestations of the optic tract syndrome relative to the causative lesion. The study population comprised of all patients with optic tract syndrome who were seen at two tertiary neuro-ophthalmology practices from 2014 to 2024. Inclusion criteria were (i) signs associated with optic tract syndrome (homonymous hemianopia and/or relative afferent pupillary defect and/or characteristic findings on peripapillary optical coherence tomography or ganglion cell analysis) and (ii) radiographically confirmed optic tract lesion. Patient records were ascertained through medical databases and reviewed. Statistical analysis was performed to identify relationships between clinical/imaging manifestations and lesion type. Fifty-six patients with optic tract syndrome were identified. The mean age was 49.4 ± 16.7 years, and 37 were female patients. Aetiologies included space-occupying lesions (

Indexed as

ganglion cell analysishomonymous hemianopiaoptical coherence tomographyoptic tract lesionsoptic tract syndrome

Identifiers

PMID41030890
PMCPMC12477588

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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.