LHON Leber’S Hereditary Optic Neuropathy

This genetic test detects mitochondrial DNA mutations associated with Leber’s Hereditary Optic Neuropathy, a hereditary condition causing sudden, painless vision loss. The test confirms diagnosis, enables genetic counseling, identifies carriers, and helps assess risk in family members. It is essential for differentiating LHON from other optic neuropathies.