Lessell S, Gise R L, Krohel G B
Arch Neurol. 1983 Jan;40(1):2-6. doi: 10.1001/archneur.1983.04050010022005.
Five young men had painless, progressive, bilateral loss of central vision with late optic atrophy. One had a family history of Leber's optic neuropathy. After being functionally blind for four to 21 months, spontaneous improvement began leading to remarkable recovery of vision in all patients. We propose that these are cases of Leber's optic neuropathy in which an unusual capacity for recovery may have been related to a lack of microvascular abnormalities in the fundi.
五名年轻男性出现无痛性、进行性双侧中心视力丧失,并伴有晚期视神经萎缩。其中一人有Leber视神经病变家族史。在功能性失明4至21个月后,所有患者均开始自发改善,视力显著恢复。我们认为这些是Leber视神经病变病例,其不同寻常的恢复能力可能与眼底缺乏微血管异常有关。