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Ｓｔａｒｇａｒｄｔ氏病为一种以中心视力下降及黄斑部双侧对称的萎缩性改变的黄斑部遗传性疾病，眼底荧光血管造影显示特异的暗脉络膜征。本文就该病的临床表现及病理学研究和近年来分子生物学检查的进展作一介绍
Stargardt’s disease is a macular hereditary disease with diminished central vision and bilateral atrophic macular degeneration, and fundus fluorescein angiography shows a specific dark choroid sign. This article on the clinical manifestations of the disease and pathology and molecular biology in recent years to make an inspection progress