Lesser R L, Albert D M, Bobowick A R, O'Brien F H
Am J Ophthalmol. 1979 Mar;87(3):317-21. doi: 10.1016/0002-9394(79)90070-9.
A 49-year-old man developed ataxia, myoclonic jerks, cortical blindness, and dementia. In 3 1/2 months, he rapidly deteriorated and died. Clinical and autopsy diagnosis confirmed Creutzfeldt-Jakob disease. The eyes were examined and bilateral optic atrophy was noted. No other ocular changes were noted. Optic atrophy had not been noted before death.
一名49岁男性出现共济失调、肌阵挛性抽搐、皮质盲和痴呆。在3个半月的时间里,他迅速恶化并死亡。临床和尸检诊断证实为克雅氏病。对其眼睛进行了检查,发现双侧视神经萎缩。未发现其他眼部变化。生前未发现视神经萎缩。