ArticleFrontiers in pediatrics2026
Case Report: Expanding the
Article in Frontiers in pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Case presentation: A full-term female infant presented with nystagmus, absent visually directed behavior, and visual responsiveness limited to bright light. Examination under general anesthesia at 15 months revealed bilateral macular pseudocoloboma, mid-peripheral termination of retinal vascularization with avascular far peripheral retina, scattered pigment clumping, and microphthalmia. Optical coherence tomography showed marked outer retinal atrophy with an irregular V-shaped foveal contour, and electroretinography demonstrated non-detectable rod and cone responses. A targeted inherited retinal dystrophy panel identified the heterozygous Conclusion: The phenotype is best interpreted as an isolated, atypical FEVR-like congenital retinal dysplasia within
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Registered trials
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.