Conditions / Genetic
retinal macular dystrophy 4
info ยท Genetic
A retinal macular dystrophy characterized by late-onset macular degeneration, with multiple drusen-like deposits, macular geographic atrophy, and choroidal neovascularization that has_material_basis_in heterozygous mutation in the CLEC3B gene on chromosome 3p2
A retinal macular dystrophy characterized by late-onset macular degeneration, with multiple drusen-like deposits, macular geographic atrophy, and choroidal neovascularization that has_material_basis_in heterozygous mutation in the CLEC3B gene on chromosome 3p21.
Signs and symptoms
- Nyctalopia
- Reduced OCT-measured foveal thickness
- Reduced visual acuity
- Choroidal neovascularization
Also known as: MCDR4