Publications by authors named "Jayaprakash Mani"
Article Synopsis
- The study focuses on genetic testing for primary mutations associated with Leber hereditary optic neuropathy (LHON) in India, analyzing 278 suspected patients from 2014-2018.
- Among the patients tested, 29.4% (82/278) were found to carry one of the three common mitochondrial DNA mutations, with the m.11778G>A mutation being the most prevalent.
- The average age of visual loss onset for those with a primary mutation was around 21 years, with typical symptoms including painless vision loss and specific visual field defects.
