Retinal and optic nerve degeneration in α-mannosidosis

Background: alpha-mannosidosis is a rare, autosomal-recessive, lysosomal storage disease caused by a deficient activity of alpha-mannosidase. Typical symptoms include intellectual, motor and hearing impairment, facial coarsening, and musculoskeletal abnormalities. Ocular pathologies reported previously were mainly opacities of the cornea and lens, strabismus, and ocular motility disorders. However, retinal and optic nerve degeneration have been rarely described. Methods: We report ocular findings of 32 patients with alpha-mannosidosis. We particularly concentrated on retinal abnormalities which we supported by posterior. segment examination, fundus photography, and Spectral-Domain optical coherence tomography (SD-OCT) imaging. Results: Tapeto retinal degeneration with bone spicule formations in the peripheral retina or macular changes were seen in three patients (9.4%) on funduscopy; of these, two with optic nerve atrophy. Eight retinal images could be obtained by OCT or fundus photography; of these, six showed thinning of the outer retinal layers on OCT. Overall, optic nerve atrophy was seen in six patients (18.8%); of these, four with partial atrophy. Two patients had partial optic nerve atrophy with no retinal abnormalities on funduscopy. Cataract was seen in two (63%), corneal haze also in two patients (6.3%). Six patients (18.8%) had manifest strabismus, four (12.5%) nystagmus, and in five patients (15.6%) impaired smooth pursuit eye movements were seen. Conclusion: Ocular pathologies are not exclusively confined to opacities of the cornea and lens or strabismus and ocular motility disorders but tapeto-retinal degeneration and optic nerve atrophy may be a common feature in alpha-mannosidosis. OCT technology helps detecting early outer retina ! thinning which can progiess with age and potentially leads to vision loss over time.