Leber Hereditary Optic Neuropathy: Visual Recovery in a Patient with the Rare m.3890G>A Point Mutation

Keyphrases

• Point mutation 100%
• Visual Recovery 100%
• Leber Hereditary Optic Neuropathy 100%
• Right Eye 66%
• Left Eye 66%
• Genome Analysis 33%
• Rare Variants 33%
• Vision Loss 33%
• Gene mutation 33%
• Uncertain Significance 33%
• Negative Testing 33%
• Complete Mitochondrial Genome 33%
• Visual Deterioration 33%
• Bilateral Optic Neuropathy 33%
• Eye Involvement 33%
• Idebenone 33%
• MT-ATP8 33%
• MT-ND1 Gene 33%
• Leigh Syndrome 33%
• Pathogenic Genes 33%

Medicine and Dentistry

• Point Mutation 100%
• Leber Hereditary Optic Neuropathy 100%
• Deterioration 33%
• Optic Neuropathy 33%
• Visual Impairment 33%
• Gene Mutation 33%
• Genome Analysis 33%
• Mitochondrial Genome 33%
• Leigh's Disease 33%
• Idebenone 33%