The intricate process of normal eye development, which occurs during the first trimester of pregnancy, involves several genes. When these genes make mistakes (called mutations), a serious eye condition can develop. Ophthalmic genetics is a much-needed and rapidly expanding field around the world. Ethnic variety, along with a high degree of consanguinity, has resulted in a global epidemic of genetic disorders. Inherited retinal disease (IRD) is the most common cause of blindness in people in their working years. Molecular diagnosis has been sped up thanks to advances in molecular genetic approaches, such as focused gene panel analysis and the use of next-generation sequencing methodologies. Likewise, developments in ocular imaging and visual function tests have enhanced our understanding of natural history, which is critical for evaluating treatment outcomes in clinical trials of potential IRD medicines.
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Title : Optic nerve orthograde axonal transport in abusive head trauma suspects
Minckler Don S, UCI, Gavin Herbert Eye Inst., United States
Title : Ultra-Widefield protocol enhances automated classification of diabetic retinopathy severity with OCT angiography
Kasra Rezaei, University of Washington, United States
Title : Lumevoq gene therapy in leber hereditary optic neuropathy
Magali Taiel, GenSight Biologics, France
Title : Various types of ocular injuries and highlights the significance of timely treatment to prevent visual loss
Gowhar Ahmad, Florence Hospital Srinagar, India
Title : Improving the quality of aftercare in patients received pars plana vitrectomy surgery
Hiu Kwan Fiona Fung, NHS Greater Glasgow and Clyde, United Kingdom
Title : Maintaining optimal oxygen saturation—the key to reduce both severe ROP & neurodisability
Hiranmoyee Das, Nazareth Hospital, India