Vision begins in the retina at the rod and cone photoreceptors, which are sensory neurons with specialized visual pigments for capturing light quanta. Most mammals have one type of rod and two ...

Mithu Tulsi Chanrai (MTC) campus, Bhubaneswar has launched a dedicated Inherited Retinal Dystrophy (IRD) Clinic to provide specialized care for patients with genetic retinal disorders. The IRD clini ...

The OCU410ST Phase 2/3 pivotal confirmatory trial represents a major advancement as Ocugen's second late-stage clinical program. Ocugen plans to submit a BLA for OCU410ST in 2027 in alignment with its ...

Edited by Jeremy Nathans, Johns Hopkins University, Baltimore, MD, and approved May 6, 2016 (received for review November 4, 2015) ...

The outer retina was avascular in all cases. There was no evidence of a FAZ in the superficial plexus. However, there was a small or partial FAZ in the deep plexus in all cases. Our OCTA findings are ...

Recent advances in retinal imaging, particularly through technologies like optical coherence tomography (OCT), have emerged as promising tools for identifying potential biomarkers for FTD and related ...

No complications or side effects were observed. Conclusion Oral treatment with 9-cis-β-carotene led to reversal of a human retinal dystrophy. This potential therapy is readily available and should be ...

Conclusion:CACNA1F mutations cause the retinal disorder, incomplete congenital stationary night blindness (CSNB2 ... Considering all features, CORDX3 is more similar to other X chromosomal cone-rod ...

These curves were developed by a computer study particularly to analyze the optical mode patterns generated within the photosensitive portions of the cones of the retina. However, they should also be ...

Repeated low-level red light (RLRL) therapy is associated with reduced cone density, particularly in the paracentral fovea, and other subtle retinal abnormalities in the eyes of children receiving the ...

This list was enriched in rod and cone photoreceptor genes and included 28 retinal disease genes, providing further evidence of a role of miRNAs in the pathology of blinding diseases. Identification ...