Color matching in autosomal dominant tritan defect
- 1 November 1981
- journal article
- Published by Optica Publishing Group in Journal of the Optical Society of America
- Vol. 71 (11) , 1327-1334
- https://doi.org/10.1364/josa.71.001327
Abstract
We evaluated color matching in 39 observers with an autosomal dominant tritan defect. Eleven tritans were dichromats with a 1° field, and only two were dichromats with an 8° field. Twenty-one of the tritan observers had normal blue–green equations with an 8° field, indicating that autosomal dominant tritans have short-wavelength-sensitive cones. Some of the tritan observers showed a shifted blue–green equation, which was ascribed to rod activity.Keywords
This publication has 16 references indexed in Scilit:
- On congenital tritanomalyVision Research, 1970
- Phenotypical variations of tritanopiaVision Research, 1966
- The inheritance of congenital tritanopia with the report of an extensive pedigreeAnnals of Human Genetics, 1964
- Combined Forms of Congenital Colour Defects : A Pedigree with Atypical Total Colour BlindnessBritish Journal of Ophthalmology, 1956
- THE FAMILIAL DISTRIBUTION OF CONGENITAL TRITANOPIAAnnals of Human Genetics, 1955
- The Characteristics of TritanopiaJournal of the Optical Society of America, 1952
- A case of tritanopyDocumenta Ophthalmologica, 1951
- The Farnsworth-Munsell 100-Hue and Dichotomous Tests for Color Vision*Journal of the Optical Society of America, 1943
- Die Tritanomalie, ein bisher unbekannter Typus anomaler TrichromasieAlbrecht von Graefes Archiv für Ophthalmologie, 1925
- Über einen Fall von angeborener beiderseitiger Tritanopie (Blaublindheit)Albrecht von Graefes Archiv für Ophthalmologie, 1906