Sirtuin 3 mutation- induced mitochondrial dysfunction and optic neuropathy: a case report

BACKGROUND: Mitochondrial optic neuropathy is characterized by painless, progressive, symmetrical central vision loss, and dyschromatopsia owing to mitochondrial dysfunction. This report documents a rare case of mitochondrial optic neuropathy due to the SIRT3 gene mutation. CASE PRESENTATION: This r...

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Detalles Bibliográficos
Autores principales: Chun, Bo Young, Choi, Jung Moon, Hwang, Su-Kyeong, Rhiu, Soolienah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037790/
https://www.ncbi.nlm.nih.gov/pubmed/36964505
http://dx.doi.org/10.1186/s12886-023-02872-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037790/
https://www.ncbi.nlm.nih.gov/pubmed/36964505
http://dx.doi.org/10.1186/s12886-023-02872-x

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