Repetitive brainstem lesions in mitochondrial DNA 11778G>A mutation of Leber hereditary optic neuropathy
- PMID: 30705974
- PMCID: PMC6348755
- DOI: 10.1016/j.ensci.2019.01.002
Repetitive brainstem lesions in mitochondrial DNA 11778G>A mutation of Leber hereditary optic neuropathy
Abstract
•LHON cases can show brainstem lesions without visual impairment.•There can be inconsistency between MRI finding and clinical symptom in LHON cases.•Auditory pathways may be often involved in LHON cases.
Keywords: Brainstem lesions; Leber hereditary optic neuropathy; Leigh syndrome; Mitochondrial disorder.
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References
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