Unexplained visual loss

被引:5
|
作者
Buono, LM
Foroozan, R
Sergott, RC
机构
关键词
blue-yellow dyschromatopsia; cecocentral scotoma; dominant optic atrophy; hereditary optic neuropathy; OPA1; gene; temporal disk pallor; tritanopia;
D O I
10.1016/j.survophthal.2003.08.007
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Dominant optic atrophy is the most common heredodegenerative optic neuropathy. Typically, patients present with slowly progressive, bilaterally decreased central visual acuity. Subtle central or cecocentral visual field defect and normal peripheral isopters are demonstrated with perimetry. A defect in blue-yellow discrimination (tritan error axis) is the most common type of dyschromatopsia, however protan and deutan axes may be superimposed. A characteristic optic disk appearance includes temporal disk pallor with excavation. An autosomal dominant inheritance pattern can often be elicited from the family history. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:626 / 630
页数:5
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