PCARE-related retinopathy

PCARE-related retinopathy is an inherited eye condition that affects the retina, the light-sensitive tissue at the back of the eye. This condition is caused by bi-allelic variants in the PCARE gene, which means that changes in both copies of the gene are involved. People with this condition may experience vision problems, as the healthy function of the retina can be compromised. Limited detailed information is available at this time on the full range of effects of this retinopathy.

Information about symptoms is currently limited for this condition.

PCARE-related retinopathy is caused by genetic changes. It is inherited in an autosomal recessive pattern, meaning that bi-allelic variants in the PCARE gene (changes in both gene copies) lead to the development of the condition. Detailed information about additional risk factors is limited.

Information about treatment is currently limited for this condition. There are no specific treatment guidelines detailed in the available sources.

Information about prognosis is currently limited for this condition. There is not enough detail available to comment on the outlook or how the condition might affect long-term vision.

Information about research is currently limited for this condition. Ongoing studies and future directions have not been detailed in the provided sources.