Leber congenital amaurosis 8

Leber congenital amaurosis 8 is a form of Leber congenital amaurosis, a group of inherited eye disorders that primarily affect vision from birth. This particular type is caused by mutations in the CRB1 gene. The condition is part of a spectrum of inherited retinal diseases where early vision loss is a common feature. The disease is identified by the specific genetic change and falls under the category of conditions that impact the retina, the light-sensitive tissue at the back of the eye. Research and understanding of the genetic causes continue to evolve as more is learned about mutations in the CRB1 gene.

Information about symptoms is currently limited for this condition.

Leber congenital amaurosis 8 is caused by a mutation in the CRB1 gene. This genetic change interferes with normal retinal development and function, leading to vision problems typically noticed at birth or in early infancy. Being an inherited condition, the mutation is passed from parents to children.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about research is currently limited for this condition.