achromatopsia 3

Achromatopsia 3 is a rare inherited condition defined by a mutation in the CNGB3 gene. This form of achromatopsia falls under a group of conditions that affect how the eye processes color. Because the mutation impairs normal gene function, the way the eyes work to interpret visual information can be altered. While the definition focuses on the genetic cause, details about how vision is affected are not fully outlined in the available information. Ongoing research may further our understanding of the condition and its impacts on vision and daily activities.

Information about symptoms is currently limited for this condition.

Achromatopsia 3 is caused by a mutation in the CNGB3 gene. This gene is important for proper functioning of the cells in the eye that contribute to vision. The mutation affects these cells, leading to the condition.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about current research is currently limited for this condition.