Patients with craniosynostosis are at high risk of developing intracranial hypertension(IH) causing papilledema and secondary optic atrophy. Diagnosing and monitoring optic neuropathy-related vision loss can be challenging because many patients with craniosynostosis have cognitive delay limiting accuracy of testing and competing causes of vision loss. PHOMS are an optical coherence tomography(OCT) feature, possibly a marker of optic neuropathy. In this study, we investigated the prevalence of PHOMS in patients with craniosynostosis and its relationship with visual function and OCT parameters.
Date
2024-03
References
Behrens CM, Malmqvist L, Jørgensen M, et al. Peripapillary Hyperreflective Ovoid Mass-like Structures (PHOMS) in Children: The Copenhagen Child Cohort 2000 Eye Study. Am J Ophthalmol. 2023;245:212-221. doi:10.1016/j.ajo.2022.09.003
Language
eng
Format
video/mp4
Type
Image/MovingImage
Source
2024 North American Neuro-Ophthalmology Society Annual Meeting
Relation is Part of
NANOS Annual Meeting: Scientific Platform: Session II