Mesh term Cone-Rod Dystrophies
Browse to parent terms:Eye Diseases, Hereditary
Retinal Dystrophies
Description
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.Search for this term in our Faculty Database
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