Leber's Hereditary Optic Neuropathy with Mitochondrial DNA Mutation G11778A: A Systematic Literature Review and Meta-Analysis.
Jiajia YuanJiaxun ZhaoChong YeLong PangXin ZhangAlvin LukYangyang DuKai Yoon FanXiaowen ZhangBin LiChangzheng ChenPublished in: BioMed research international (2023)
The G11778A mutation is a prevalent mitochondrial DNA mutation accounting for over half of LHON cases with three primary mutations. Spontaneous visual recovery is rare, and no effective treatment is currently available.