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A Rare ND5 Mutation Causing Leber's Hereditary Optic Neuropathy.
Bhadra U Pandya1, Amir R Vosoughi2, Aaditeya Jhaveri1
1Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Case Reports in Ophthalmology
|March 20, 2023
Summary
This case report details a rare ND5 gene mutation (m.13528A>G) causing Leber's hereditary optic neuropathy (LHON). The study expands understanding of this mutation's clinical presentation and patient outcomes.
Area of Science:
- Genetics
- Ophthalmology
- Neurology
Background:
- Leber's hereditary optic neuropathy (LHON) is a mitochondrial disease.
- Mutations in the ND5 gene are rarely linked to LHON.
- The specific m.13528A>G mutation is infrequently reported.
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