Late onset dominant cone dystrophy with early blue cone involvement.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 1583655.
- Also identified by PMC identifier 1015947.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
A dominant cone dystrophy spanning seven generations was found in a pedigree from the Netherlands. The onset of the decline of visual acuity started after the age of 20, while a near complete absence of blue cone function (a so-called tritan defect) already existed before the presence of any ophthalmological abnormalities.
Medical subject headings
- Color Vision Defects
- Retinitis Pigmentosa