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September 16, 2025Journal of Neuro-Ophthalmology

An Additional Case of Leber Hereditary Optic Neuropathy With G9804A Mutation

Samir Cayenne Maryam Naser Sanjana Jaiswal Elizabeth Arogundade Peter William Mortensen Andrew G. Lee

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Key Points

This case adds to the understanding of leber hereditary optic neuropathy and its genetic underpinnings.
The g9804a mutation identified may serve as a marker for diagnosis and understanding of the condition.
Genetic analysis was key in diagnosing this patient with leber hereditary optic neuropathy associated with g9804a.
The findings enhance existing knowledge on optic neuropathy, suggesting genetic counseling may be necessary.

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Implication

Additional case highlights the role of the g9804a mutation in leber hereditary optic neuropathy.

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Cite This Study

Cayenne et al. (2025) studied this question.

synapsesocial.com/papers/68d45e6231b076d99fa5ec6a https://doi.org/10.1097/wno.0000000000002397

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