Genetically heterogeneous and sometimes syndromic (e.g., BARDET BIEDL SYNDROME; and SPINOCEREBELLAR ATAXIA TYPE 7) retinopathies with initial RETINAL CONE involvement. They are characterized by decreased VISUAL ACUITY; COLOR VISION DEFECTS; progressive loss of peripheral vision and night blindness.
Also Known As:
Cone-Rod Degenerations; Cone-Rod Dystrophy; Cone-Rod Dystrophy 2; Cone-Rod Retinal Dystrophy; Retinal Cone-Rod Dystrophy; Rod Cone Dystrophies; Cone Rod Degenerations; Cone Rod Dystrophies; Cone Rod Dystrophy; Cone Rod Dystrophy 2; Cone Rod Retinal Dystrophy; Cone-Rod Degeneration; Cone-Rod Dystrophies, Retinal; Cone-Rod Dystrophy, Retinal; Cone-Rod Retinal Dystrophies; Retinal Cone Rod Dystrophy; Retinal Cone-Rod Dystrophies; Retinal Dystrophies, Cone-Rod; Retinal Dystrophy, Cone-Rod; Rod Cone Dystrophy; Rod-Cone Dystrophies; Rod-Cone Dystrophy