Ophthalmic Genetics
Ophthalmic genetics includes determination of patterns and risks of inheritance and development of treatments for genetic diseases. Vitamin A deficiency is the leading cause of preventable blindness in children worldwide and results in a well-recognized ocular phenotype. It is also includes the several technique in correcting the defective gene by using application of biotechnology techniques such as gene therapy. Ophthalmic genetics or ophthalmic gene therapy can process through by following methods like ocular gene transfer methods. They have been several diseases which have been cured by gene therapy like retinitis pigmentosa and ARMD.
- Abnormalities of Nuclear or Mitochondrial DNA
- Autosomal dominant disorders
- Autosomal recessive disorders
- X-linked recessive disorders
- Matrilineal inheritance
- Chromosomal Abnormalities
Related Conference of Ophthalmic Genetics
March 23-24, 2026
10th International Conference & Expo on Euro Optometry and Vision Science
London, UK
Ophthalmic Genetics Conference Speakers
Recommended Sessions
- Clinical Ophthalmology
- Cornea and External Diseases
- Diagnostics and Imaging Tools in Ophthalmology
- Eye Surgery
- Glaucoma
- Neuro Ophthalmology
- Ocular Oncology
- Ocular Pharmacology
- Ophthalmic Genetics
- Ophthalmic Nursing
- Ophthalmology Management
- Pediatric Ophthalmology
- Smartphones, Eyestrain and Discomfort
- Vision Therapy
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