Stargardt disease is an inherited retinal condition. With an incidence of 8-10 per 100,000 persons, it is the most common juvenile macular degeneration. The majority of cases present in an autosomal recessive fashion and are due to mutations in the ABCA4 gene. The condition tends to manifest at an early age; however, large amounts of heterogeneity are seen in terms of genotype and phenotype thus the condition can have a later onset with variable clinical findings. The purpose of this case report is to present two different phenotypic presentations of Stargardt disease that were diagnosed based on a combination of multimodal imaging and genetic testing. A comprehensive review of the etiology, clinical features, treatment and management of the disease is also presented. [ABSTRACT FROM AUTHOR]