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Further advances in the diagnosis and treatment of Leber’s Hereditary Optic Neuropathy – a review

Leber’s Hereditary Optic Neuropathy (LHON), is one of the most frequent mitochondrial diseases characterized by Retinal Ganglion Cells degeneration. Pathogenic gene mutations in LHON induces mitochondrial impairment, which in turn leads to insufficient mitochondrial ATP production. The pathologic ha...

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Detalles Bibliográficos
Autores principales: Tăbăcaru, Bogdana, Stanca, Horia Tudor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Romanian Society of Ophthalmology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022147/
https://www.ncbi.nlm.nih.gov/pubmed/35531455
http://dx.doi.org/10.22336/rjo.2022.4

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