Dobbie J G, Fetkenhour C L, Shoch D
Trans Am Ophthalmol Soc. 1975;73:141-52.
A family with a unique hereditary macular dystrophy is presented. The disorder is transmitted as an autosomal dominant trait having high penetrance and variable expression. The characteristics of this dystrophy are: childhood onset; nonprogressive areolar depigmentation of the central macula; and with the exception of one eye with a macular hemorrhage, normal vision acuity and retinal-function studies.
本文报告了一个患有独特遗传性黄斑营养不良的家族。该疾病以常染色体显性性状遗传，具有高外显率和可变表达。这种营养不良的特征为：儿童期发病；中央黄斑区出现非进行性乳晕色素脱失；除一只眼睛有黄斑出血外，视力和视网膜功能检查正常。
