Leber hereditary optic neuropathy with chorea and dementia resembling Huntington disease

MeSH terms

• Adult
• Atrophy
• Basal Ganglia / blood supply
• Basal Ganglia / diagnostic imaging
• Caudate Nucleus / pathology
• Chorea / diagnosis*
• Chorea / genetics
• DNA, Mitochondrial / genetics
• Dementia / diagnosis*
• Diagnosis, Differential
• Disease Progression
• Female
• Genetic Heterogeneity
• Humans
• Huntington Disease / diagnosis*
• Huntington Disease / genetics
• Magnetic Resonance Imaging
• Male
• NADH Dehydrogenase / genetics
• Occipital Lobe / blood supply
• Occipital Lobe / diagnostic imaging
• Occipital Lobe / pathology
• Optic Atrophy, Hereditary, Leber / diagnosis*
• Optic Atrophy, Hereditary, Leber / genetics
• Optic Atrophy, Hereditary, Leber / pathology
• Parietal Lobe / blood supply
• Parietal Lobe / diagnostic imaging
• Parietal Lobe / pathology
• Point Mutation
• Syndrome
• Tomography, Emission-Computed, Single-Photon