GUCY2D-related recessive retinopathy

GUCY2D-related recessive retinopathy is a condition that affects the retina, the light-sensitive tissue at the back of the eye. This condition is caused by changes in both copies of the GUCY2D gene, which are known as biallelic variants. As a result, the normal function of the retina is impaired, which may affect vision in people with this condition. Because this retinopathy is linked to specific genetic changes, understanding the role of the GUCY2D gene can help clarify how the condition develops. While more detailed information may be available from further research, the key point is that these genetic changes lead to a form of retinal disease affecting the function of the eyes.

Information about symptoms is currently limited for this condition.

This condition is caused by biallelic variants in the GUCY2D gene. In people with this condition, changes in both copies of this gene lead to a retinopathy. This genetic cause is the primary factor behind the development of the disease.

Information about treatment options 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.