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 …

Oct 4, 2024 · Cone-rod dystrophy is a genetic condition that causes light-sensitive cells in your retina to break down. It eventually leads to loss of color, central and peripheral vision, and, ultimately, blindness.

Cone dystrophies (COD) and cone-rod dystrophies (CORD) are a subset of inherited retinal diseases (IRDs) characterized by primary cone degeneration with variable secondary rod involvement. 1 Due …

Cone-rod dystrophy is a group of related eye disorders that causes vision loss, which becomes more severe over time. These disorders affect the retina, which is the layer of light-sensitive tissue at the …

As the condition progresses, individuals may develop involuntary eye movements (nystagmus). There are more than 30 types of cone-rod dystrophy, which are distinguished by their genetic cause and …

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.

A rare genetic isolated inherited retinal disorder characterized by primary cone degeneration with significant secondary rod involvement, with a variable fundus appearance.

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 …

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.