Neurofibromatosis type 2 (NF2) is a genetically determined tumor-predisposing syndrome. Ocular manifestations include cataracts, epiretinal membranes, retinal hamartomas, optic disk gliomas, and nerve sheath meningiomas. Moreover, edema, optical atrophy, motility disorders, pupil lid dysfunction, neurotrophic keratitis can be observed as indirect signs. An observational study was conducted with...