congenital stationary night blindness autosomal dominant 3

A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the GNAT1 gene on chromosome 3p21.

Signs and symptoms

• Early-onset non-progressive night blindness

Also known as: CSNBAD3; Nougaret type congenital stationary night blindness