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Cone-rod dystrophy (CRD) is a group of inherited eye disorders that affect the light sensitive cells of the retina called the cones and rods. People with this condition experience vision loss over time as the cones and rods deteriorate.
Cone-rod dystrophy is a group of related eye disorders that causes vision loss, which becomes more severe over time. Explore symptoms, inheritance, genetics of this condition.
Jun 14, 2021 · Cone-rod dystrophies are a group of rare eye disorders that affect both the cone and rod cells of the retina. In some cases, individuals experience deterioration of the cone cells more severely than the rod cells.
A cone dystrophy is an inherited ocular disorder characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision . Presentation. The most common symptoms of cone dystrophy are vision loss (age of onset ranging from the late teens to the sixties), sensitivity to bright lights, and poor color vision.
Cone-Rod dystrophy is a group of rare and inherited retinal degenerations (IRDs) which affect the light-sensing rod and cone photoreceptor cells in the retina, the tissue layer which lines the back of the eye. Cone cells are most concentrated at the centre of the retina, in the macula.
Learn about cone rod dystrophy, a group of inherited diseases that cause deterioration of the retina's light-sensitive cells. Understand its impact on vision and available treatments.
Cone dystrophy stops the cones working, leading to loss of central and colour vision. People with stationary dystrophy have the same level of sight loss from birth or early childhood. Progressive dystrophy develops later and sight is lost gradually over time.
