학술논문

Late-onset Stargardt disease
Document Type
article
Source
American Journal of Ophthalmology Case Reports, Vol 26, Iss , Pp 101429- (2022)
Subject
ABCA4 gene
Differential diagnosis
Hereditary macular dystrophy
Late-onset stargardt disease
Macular degeneration
Vitamin A
Ophthalmology
RE1-994
Language
English
ISSN
2451-9936
Abstract
Purpose: To report a case of late-onset Stargardt disease, discuss the differential diagnosis, and review the role of vitamin A supplementation in Stargardt disease. Observations: A 60-year-old man presented with blurry vision in the right eye for the past two years. Current medications included a daily multivitamin containing vitamin A and age-related eye disease study vitamins. Examination revealed bilateral macular atrophy and scattered yellow flecks which were intensely hyperautofluorescent. Fluorescein angiography revealed a dark choroid. Full-field electroretinogram showed normal rod and cone responses, and genetic testing revealed two pathogenic ABCA4 gene variations confirming the diagnosis of late-onset Stargardt disease. Conclusions: Stargardt disease is typically described in young patients but may develop later in adulthood and masquerade as age-related macular degeneration and a number of other conditions. Though the evidence is limited, there is concern that high-dose vitamin A supplementation could lead to progression of Stargardt disease. Avoidance of high-dose vitamin A supplementation should be discussed with Stargardt disease patients.