Understanding Leber’s Hereditary Optic Neuropathy (LHON)
Leber’s hereditary optic neuropathy is a rare genetic eye disorder that primarily affects young adults, leading to sudden vision loss. This condition is caused by mutations in mitochondrial DNA, which impair the function of retinal ganglion cells. As a result, central vision deteriorates rapidly, often in both eyes. Early diagnosis of Leber’s hereditary optic neuropathy is crucial for better visual outcomes. Read more: https://www.theconsumersfeedba....ck.com/guestpost/ide

Understanding Leber’s Hereditary Optic Neuropathy
Leber’s Hereditary Optic Neuropathy is a rare genetic eye disorder that primarily affects young adults, leading to sudden vision loss. Caused by mutations in mitochondrial DNA, LHON disrupts the normal function of retinal ganglion cells. Vision loss often begins in one eye and progresses to the other within weeks or months. Early symptoms may include blurred vision and difficulty distinguishing colors.Visit us: https://idebenone.org/