Ophthalmogenetics and Gene Therapy
Ophthalmic hereditary qualities are worried about the hereditary commitment to ophthalmic illness, including assurance of examples and dangers of legacy, and in addition finding, visualization, and advancement of medications for hereditary variations from the norm. The advances in gene therapy maintain extensive promise for the cure of ophthalmic conditions. Gene therapy is additionally in a position to deal with primary open-angle glaucoma (POAG) in animal models, and research show it is economically viable. Genes may additionally be delivered into cells in vitro or in vivo making use of viral or non-viral vectors. Recent technical advances have led to the demonstration of the molecular basis of a range of ocular diseases.
- Genetics of Myopia Development
- Gene Therapy
- Usher syndrome
- Familial exudative vitreal retinopathy
- Retinoblastoma
- Leber hereditary optic neuropathy (LHON)
- Optic atrophy
- Genetics of Myopia Development
Related Conference of Ophthalmogenetics and Gene Therapy
September 16-17, 2025
20th International Conference on Ophthalmology and Vision Science
Amsterdam, Netherlands
March 23-24, 2026
10th International Conference & Expo on Euro Optometry and Vision Science
London, UK
Ophthalmogenetics and Gene Therapy Conference Speakers
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