ArticlePediatric investigation2025
Horner syndrome in a pediatric patient.
Article in Pediatric investigation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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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.
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Who cites it
1 citing paper in PubMed.
- Horner syndrome in a pediatric patient.Pediatric investigation · 2025Article
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Horner syndrome (HS) is a rare neurological disorder arising from disruption of the oculosympathetic pathway. Pediatric HS is uncommon and may be congenital, but underlying sinister causes need to be excluded. Case presentation: An 18-week-old boy presented with right peri-orbital swelling, initially thought to be pre-septal cellulitis. Further ophthalmic review revealed a right-sided HS. Imaging identified a probable cervical neuroblastoma, leading to an urgent referral to oncology. Conclusion: Early recognition of pediatric HS is crucial as it may signal underlying malignancies like neuroblastoma. Atypical presentations with sequential or intermittent symptoms make diagnosis challenging. Comprehensive imaging and multidisciplinary care ensure timely diagnosis and management.
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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 Socratic graph.