Usher Syndrome is a rare inherited genetic disorder that affects both hearing and vision. It is the most common condition that causes combined deafness or hearing loss with progressive vision impairment due to Retinitis Pigmentosa (RP). In some individuals, Usher Syndrome also affects balance, making...
Leber Congenital Amaurosis (LCA) is a rare inherited retinal disorder that causes severe vision impairment or blindness from birth or during the first few months of life. It is one of the earliest forms of inherited retinal dystrophy and occurs due to genetic mutations that...
Choroideremia is a rare inherited retinal disorder that causes progressive vision loss due to the gradual degeneration of the retina, retinal pigment epithelium (RPE), and choroid—the vascular layer that supplies oxygen and nutrients to the retina. The condition primarily affects males because it is inherited...
Retinitis Pigmentosa (RP) is a group of inherited retinal disorders that gradually affect the retina's ability to process light, leading to progressive vision loss over time. Because the condition usually develops slowly, many people fail to recognize its early symptoms until daily activities become increasingly...
Retinitis Pigmentosa (RP) is a group of inherited retinal disorders that gradually affect the light-sensitive cells of the retina. The condition primarily damages rod photoreceptor cells, which are responsible for night vision and peripheral vision, and later affects cone cells that support central vision and...
