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.
Inga svenska synonymer finns.
Cone Rod Dystrophies — Cone-Rod Dystrophy — Cone Rod Dystrophy — Cone-Rod Degenerations — Cone-Rod Degeneration — Cone Rod Degenerations — Cone-Rod Retinal Dystrophy — Cone-Rod Retinal Dystrophies — Cone Rod Retinal Dystrophy — Retinal Dystrophies, Cone-Rod — Retinal Dystrophy, Cone-Rod — Retinal Cone-Rod Dystrophy — Cone-Rod Dystrophies, Retinal — Cone-Rod Dystrophy, Retinal — Retinal Cone-Rod Dystrophies — Retinal Cone Rod Dystrophy — Cone-Rod Dystrophy 2 — Cone Rod Dystrophy 2 — Rod-Cone Dystrophy — Rod-Cone Dystrophies — Rod Cone Dystrophies — Rod Cone Dystrophy