论文部分内容阅读
Stargardt病是一种并不常见的遗传性黄斑萎缩性变性疾病,多数为常染色体隐性遗传,少数为显性遗传。1909年初Stargardt首次描述了这此病并以其名字命名。Stargardt病的眼底特征性表现为椭圆形黄斑萎缩区和/或黄斑区周围的黄色斑点。此病严重影响视力但目前尚无有效治疗方法。病
Stargardt disease is an uncommon hereditary disease of the macular atrophy, most of which are autosomal recessive and a few are dominant. Stargardt first described the disease in 1909 and named after it. The fundus of Stargardt’s disease is typically characterized by yellow spots around the oval macular atrophy and / or around the macula. The disease seriously affects eyesight but there is no effective treatment. disease