Achromatopsia, also known as rod monochromacy, is a medical syndrome that exhibits symptoms relating to five conditions, most notably monochromacy. Historically, the name referred to monochromacy in general, but now typically refers only to an autosomal recessive congenital color vision condition.

Achromatopsia is an inherited vision disorder affecting your ability to perceive color. The condition also affects vision quality. Symptoms can be severe and interfere with everyday life.

Achromatopsia is a rare, bilateral inherited retinal degeneration affecting all three types of cone photoreceptor cells that results in the absecnce of color discrimination. The disease can be complete with total lack of cone function, also known as rod monochromatism, or blue-cone (S cone) monochromatism.

2023年4月3日 · Achromatopsia is a condition that affects both eyes. It generally does not progress, meaning that a person’s vision typically does not worsen over time due to this disorder. Like most types of color blindness, achromatopsia results from a problem within the retina.

Achromatopsia is a condition characterized by a partial or total absence of color vision. People with complete achromatopsia cannot perceive any colors; they see only black, white, and shades of gray. Incomplete achromatopsia is a milder form of …

2004年6月24日 · Achromatopsia is characterized by reduced visual acuity, pendular nystagmus, increased sensitivity to light (photophobia), a small central scotoma, eccentric fixation, and reduced or complete loss of color discrimination.

A rare autosomal recessive retinal disorder characterized by color blindness, nystagmus, photophobia, and severely reduced visual acuity due to the absence or impairment of cone function. Summary.

Achromatopsia is an eye problem where it is hard to see and hard to see colors. This is because a part of the eye called the retina does not work well. People with this issue have blurry vision and mostly see black, white, and gray.

2020年10月8日 · Achromatopsia is an inherited retinal condition causing extreme light sensitivity (i.e., day blindness), as well as reduced visual acuity and color discrimination. Achromatopsia is caused by mutations in any of several genes.

Achromatopsia, commonly known as total color blindness, is a rare hereditary visual disorder characterized by the absence of color discrimination and a range of other visual impairments. This condition affects approximately 1 in 30,000 individuals worldwide.