IMPG1-related dominant retinopathy

IMPG1-related dominant retinopathy is a type of eye disease caused by an autosomal dominant variant in the IMPG1 gene. This condition affects the retina, the light-sensitive tissue at the back of the eye, leading to retinopathy, which is a disorder of the retina. People with this condition have one altered copy of the IMPG1 gene. Details about how the gene change leads to retinal problems are limited, but the basic definition indicates that the variant in the IMPG1 gene plays a key role in the development of this retinopathy.

Information about symptoms is currently limited for this condition.

IMPG1-related dominant retinopathy is caused by a genetic variant in the IMPG1 gene inherited in an autosomal dominant pattern. This means that only one copy of the altered gene can cause the condition. The gene variant affects the retina, although further details on the mechanism are limited in the available information.

Information about treatment options is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about current research and future directions is currently limited for this condition.