Late Development of Vitelliform Lesions and Flecks in a Patient With Best Disease
Open Access
- 1 November 2005
- journal article
- case report
- Published by American Medical Association (AMA) in Archives of Ophthalmology (1950)
- Vol. 123 (11) , 1588-1594
- https://doi.org/10.1001/archopht.123.11.1588
Abstract
ObjectiveTo provide the clinicopathologic findings of a patient who developed the clinical characteristics of Best disease (typically considered a juvenile macuKeywords
This publication has 15 references indexed in Scilit:
- The vitelliform macular dystrophy protein defines a new family of chloride channelsProceedings of the National Academy of Sciences, 2002
- Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease)Human Molecular Genetics, 1998
- Identification of the gene responsible for Best macular dystrophyNature Genetics, 1998
- The gene for Best's macular dystrophy is located at 11q13 in a Swedish familyClinical Genetics, 1992
- Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13Nature Genetics, 1992
- Histopathologic Findings in Best's Vitelliform Macular DystrophyArchives of Ophthalmology (1950), 1988
- A Histopathologic Study of Best's Macular DystrophyArchives of Ophthalmology (1950), 1982
- Histopathology of Best's Macular DystrophyArchives of Ophthalmology (1950), 1982
- Long-term Evaluation of Patients with Best's Vitelliform DystrophyOphthalmology, 1981
- Vitelliform Dystrophy in a 64-Year-Old ManAmerican Journal of Ophthalmology, 1976