Article
Chromosome 19q cone-rod retinal dystrophy. Ocular phenotype.
Archives of ophthalmology (Chicago, Ill. : 1960) - 1 Feb 1995
Evans K, Duvall-Young J, Fitzke F W, Arden G B, Bhattacharya S S, Bird A C
Abstract excerpt
OBJECTIVE: To describe the phenotype in a family with dominantly inherited cone-rod dystrophy with chromosome assignment to a 19q locus, and to correlate this with current classifications of this retinal dystrophy. DESIGN: A detailed clinical examination including Goldmann perimetry was undertake...
Topics
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Child
- Chromosomes, Human, Pair 19
- Dark Adaptation
- Electroretinography
- Female
- Fundus Oculi
- Genetic Linkage
- Humans
- Male
- Middle Aged
- Night Blindness
- Pedigree
- Phenotype
- Photoreceptor Cells