A novel case of Horner syndrome as the presenting sign of craniosynostosis
We present a novel case of Horner syndrome as the presenting sign of craniosynostosis associated with elevated intracranial pressure. A 10-year-old boy presenting for strabismus follow-up was noted to have new-onset anisocoria, greater in the dark, and mild right upper eyelid ptosis. Apraclonidine testing was concerning for Horner syndrome. Neuroimaging demonstrated previously undiagnosed sagittal craniosynostosis with tortuous optic nerves and large cerebrospinal fluid spaces around both optic nerves.
Source: Journal of AAPOS - Category: Opthalmology Authors: Nina Diklich, Sugi Panneerselvam, Nathalie E. Perez, Michelle Falcone, Kara M. Cavuoto Tags: Short Report Source Type: research