Oguchi disease-1

A congenital stationary night blindness characterized by congenital static night blindness, a golden or gray-white discoloration of the fundus that disappears in the dark-adapted state and typically normal function of all other visual functions that has_materi

A congenital stationary night blindness characterized by congenital static night blindness, a golden or gray-white discoloration of the fundus that disappears in the dark-adapted state and typically normal function of all other visual functions that has_material_basis_in homozygous or compound heterozygous mutation in the SAG gene on chromosome 2q37.

Signs and symptoms

• Early-onset non-progressive night blindness
• Mizuo phenomenon

Also known as: CSNBO1; congenital stationary night blindness Oguchi type 1