Cone-Rod Dystrophies


Cone Rod Degenerations

Cone Rod Dystrophies

Cone Rod Dystrophy

Cone Rod Dystrophy 2

Cone Rod Retinal Dystrophy

Cone-Rod Degeneration

Cone-Rod Degenerations

Cone-Rod Dystrophies, Retinal

Cone-Rod Dystrophy

Cone-Rod Dystrophy 2

Cone-Rod Dystrophy, Retinal

Cone-Rod Retinal Dystrophies

Cone-Rod Retinal Dystrophy

Retinal Cone Rod Dystrophy

Retinal Cone-Rod Dystrophies

Retinal Cone-Rod Dystrophy

Retinal Dystrophies, Cone-Rod

Retinal Dystrophy, Cone-Rod

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.