Ishihara Electronic Color Blindness Test: an Evaluation Study
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Sensitivities in Older Eyes with Good Acuity: Cross-Sectional Norms
Sensitivities in Older Eyes With Good Acuity: Cross-Sectional Norms Alvin Eisner,*f Susan A. Fleming,*! Michael L. Kleins and W. Manning Mauldinf We measured several indices of foveal visual function for a large group of people aged 60 and older. The data reported in this paper are from individuals who had good acuity in each eye and met a number of other criteria for good ocular health. For each index, we described the rate of cross-sectional change with age using linear regression statistics. We found age-related change for eyes having 20/20 or better acuity to exist for several different indices. Sensitivity mediated by the blue-sensitive cones decreased with age, as expected. However, the rate of decrease was faster for females than for males. At least part of the difference was associated with different rates of lenticular change. Absolute sensitivity at long wavelengths also decreased with age, but at the same rate for each sex. Rayleigh color matches changed with age in a manner consistent with underlying age-related decreases of effective foveal cone photopigment density. However, not all indices showed age-dependent changes. For instance, the time constant describing the rate of photopic dark adaptation did not appear to change with age. Invest Ophthalmol Vis Sci 28:1824-1831, 1987 Human visual function changes with age. Cross- criteria for good ocular health in each eye. In particu- sectional age-related changes have been reported for lar, we have tested people having good acuity in each Snellen acuity,1 spatial2"4 and temporal4 contrast sen- eye. -
ERG), Molecular and Behavioral Studies
Vision Research 38 (1998) 3377–3385 Severity of color vision defects: electroretinographic (ERG), molecular and behavioral studies M.A. Crognale a,b,*, D.Y. Teller a,c, A.G. Motulsky d,e, S.S. Deeb d,e a Department of Psychology, Uni6ersity of Washington, Box 351525, Seattle, WA 98195-1525, USA b Department of Ophthalmology, Uni6ersity of Washington, Seattle, WA, USA c Department of Physiology/Biophysics, Uni6ersity of Washington, Seattle, WA, USA d Department of Genetics, Uni6ersity of Washington, Seattle, WA, USA e Department of Medicine, Uni6ersity of Washington, Seattle, WA, USA Received 10 July 1997; received in revised form 29 October 1997 Abstract Earlier research on phenotype/genotype relationships in color vision has shown imperfect predictability of color matching from the photopigment spectral sensitivities inferred from molecular genetic analysis. We previously observed that not all of the genes of the X-chromosome linked photopigment gene locus are expressed in the retina. Since sequence analysis of DNA does not necessarily reveal which of the genes are expressed into photopigments, we used ERG spectral sensitivities and adaptation measurements to assess expressed photopigment complement. Many deuteranomalous subjects had L, M, and L–M hybrid genes. The ERG results showed that M pigment is not present in measurable quantities in deutan subjects. Using these results to determine gene expression improved the correlations between inferred pigment separation and color matching. Furthermore, we found a subject who had normal L and M genes and normal proximal promoter sequences, yet he had a single photopigment (M) by ERG and tested as a protanope. These results demonstrate the utility of ERG measurements in studies of molecular genetics of color vision deficiencies, and further support the conclusion that not all genes are expressed in color deficient subjects. -
The Genetics of Normal and Defective Color Vision
Vision Research xxx (2011) xxx–xxx Contents lists available at ScienceDirect Vision Research journal homepage: www.elsevier.com/locate/visres Review The genetics of normal and defective color vision Jay Neitz ⇑, Maureen Neitz University of Washington, Dept. of Ophthalmology, Seattle, WA 98195, United States article info a b s t r a c t Article history: The contributions of genetics research to the science of normal and defective color vision over the previ- Received 3 July 2010 ous few decades are reviewed emphasizing the developments in the 25 years since the last anniversary Received in revised form 25 November 2010 issue of Vision Research. Understanding of the biology underlying color vision has been vaulted forward Available online xxxx through the application of the tools of molecular genetics. For all their complexity, the biological pro- cesses responsible for color vision are more accessible than for many other neural systems. This is partly Keywords: because of the wealth of genetic variations that affect color perception, both within and across species, Color vision and because components of the color vision system lend themselves to genetic manipulation. Mutations Cone photoreceptor and rearrangements in the genes encoding the long, middle, and short wavelength sensitive cone pig- Colorblindness Cone mosaic ments are responsible for color vision deficiencies and mutations have been identified that affect the Opsin genes number of cone types, the absorption spectra of the pigments, the functionality and viability of the cones, Evolution and the topography of the cone mosaic. The addition of an opsin gene, as occurred in the evolution of pri- Comparative color vision mate color vision, and has been done in experimental animals can produce expanded color vision capac- Cone photopigments ities and this has provided insight into the underlying neural circuitry. -
Comparing Color Vision Testing Using the Farnsworth-Munsell 100-Hue, Ishihara Compatible, and Digital TCV Software Rachel A
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by CommonKnowledge Pacific nivU ersity CommonKnowledge College of Optometry Theses, Dissertations and Capstone Projects 4-23-2015 Comparing Color Vision Testing Using the Farnsworth-Munsell 100-Hue, Ishihara Compatible, and Digital TCV Software Rachel A. Murphy Pacific nU iversity, [email protected] Recommended Citation Murphy, Rachel A., "Comparing Color Vision Testing Using the Farnsworth-Munsell 100-Hue, Ishihara Compatible, and Digital TCV Software" (2015). College of Optometry. Paper 9. http://commons.pacificu.edu/opt/9 This Thesis is brought to you for free and open access by the Theses, Dissertations and Capstone Projects at CommonKnowledge. It has been accepted for inclusion in College of Optometry by an authorized administrator of CommonKnowledge. For more information, please contact [email protected]. Comparing Color Vision Testing Using the Farnsworth-Munsell 100-Hue, Ishihara Compatible, and Digital TCV Software Abstract It is crucial that eye care professionals be able to provide quick, accurate, and complete testing of color vision, both to enhance the lives of patients and to satisfy the requirements laid out by industry standards. With the growing popularity of the use of digital equipment in offices, there is a natural progression to digital color vision screening tests, which have the advantage of being fast, inexpensive, and readily portable with automated scoring for greater consistency. Few studies have sought to validate specific digital tests. The aim of this study is to compare two traditionally accepted manual tests for detecting congenital color vision deficiency (CCVD) with analogous digital versions. -
A New Test System and a New Cause for Acquired Foveal Color-Vision Deficiency
International Journal of Ophthalmology & Visual Science 2016; 1(1): 8-19 http://www.sciencepublishinggroup.com/j/ijovs doi: 10.11648/j.ijovs.20160101.12 A New Test System and a New Cause for Acquired Foveal Color-Vision Deficiency Terry Bahill Systems and Biomedical Engineering, University of Arizona, Tucson Arizona, USA Email address: [email protected] To cite this article: Terry Bahill. A New Test System and a New Cause for Acquired Foveal Color-vision Deficiency. International Journal of Ophthalmology & Visual Science. Vol. 1, No. 1, 2016, pp. 8-19. doi: 10.11648/j.ijovs.20160101.12 Received: August 22, 2016; Accepted: November 8, 2016; Published: December 2, 2016 Abstract: The purpose of this paper is to show a new cause of a macular scotoma and an anomalous acquired color-vision deficiency in the clinical fovea caused by retina detachments and subsequent surgeries. This deficiency was measured with a visual test system composed of multiple lasers, a white light beam and dozens of targets that were projected on a computer monitor and printed on paper. Lasers were used, because they produce small monochromatic target dots, 0.07 degrees of visual angle (6 mm) in diameter. The outputs of the system were the subject’s perceived color matches. In experiments with small dots of laser light, colors were judged correctly by the right eye (OD): however, the left eye (OS) could not distinguish colors. For example, a green laser dot appeared green to his OD and white to his OS. Perceived color in the abnormal OS depended on the target’s hue, saturation, luminance, wavelength, size and position on the fovea. -
Defective Color Vision and Its Inheritance by George Wald*
DEFECTIVE COLOR VISION AND ITS INHERITANCE BY GEORGE WALD* BIOLOGICAL LABORATORIES, HARVAkRD IJNIVERSITY We owe the first accurate description of color blindness to the chemist John Dalton, who in 1798 characterized his own condition in the words 'persons in general dis- tinguish six kinds of colour in the solar image; namely, red, orange, yellow, green, blue, and purple.... To me it is quite otherwise:-I see only two, or at most three, distinctions. These I should call yellow and blue; or yellow, blue, and purple. MiIy yellow comprehends the red, orange, yellow, and green of others; and my blue and purple coincide with theirs. That part of the image which others call red, ap- pears to me little more than a shade, or defect of light....". In this superb paper, Dalton set all the main themes for the study of color blindness. He pointed out that his vision had always been this way; that his brother had the same defect; that he knew of nearly 20 such cases, all male; and that in all but perhaps one in- stance the parents and children of such persons had normal vision.' Dalton thought the trouble to be that his vitreous humor was tinted blue, and so did not pass red light; but Thomas Young said of this: ". it is much more simple to suppose the absence or paralysis of those fibers of the retina which are calculated to perceive red."2 Dalton held to his own view, and the argument was settled only by autopsy at his death in 1842, when his eyes were found to be normally trans- parent to red light.3 Color blindness is still called daltonism throughout Europe; but Young's explanation, that it involves the loss of one of three normal color mechanisms, remained for many years the dominant theory of this condition. -
Cortical Color Loss and the Chromatic Visual Evoked Potential Department of Psychology, Program in Cognitive and # Michael A
Journal of Vision (2013) 13(10):15, 1–11 http://www.journalofvision.org/content/13/10/15 1 The locus of color sensation: Cortical color loss and the chromatic visual evoked potential Department of Psychology, Program in Cognitive and # Michael A. Crognale Brain Sciences, University of Nevada, Reno, NV, USA $ Department of Psychology, Program in Cognitive and Chad S. Duncan Brain Sciences, University of Nevada, Reno, NV, USA $ Department of Psychology, Program in Cognitive and Hannah Shoenhard Brain Sciences, University of Nevada, Reno, NV, USA $ Department of Psychology, Program in Cognitive and Dwight J. Peterson Brain Sciences, University of Nevada, Reno, NV, USA $ Department of Psychology, Program in Cognitive and # Marian E. Berryhill Brain Sciences, University of Nevada, Reno, NV, USA $ Color losses of central origin (cerebral achromatopsia and dyschromatopsia) can result from cortical damage Introduction and are most commonly associated with stroke. Such cases have the potential to provide useful information Color vision can be disrupted or lost by a number of regarding the loci of the generation of the percept of causes, the most common being genetic mutations. color. One available tool to examine this issue is the Achromatopsia is a condition wherein the percept of chromatic visual evoked potential (cVEP). The cVEP has colors is absent. Much more common is dyschroma- been used successfully to objectively quantify losses in topsia wherein there is a partial loss of color capacity. color vision capacity in both congenital and acquired Many cases of achromatopsia and most cases of deficiencies of retinal origin but has not yet been applied to cases of color losses of cortical origin. -
Comparison of Farnsworth and Lanthony D-15 Color Vision Tests to an Computerized Color Vision Cap Rearrangement Test James Kundart Pacific Nu Iversity
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by CommonKnowledge Pacific nivU ersity CommonKnowledge Faculty Scholarship (COO) College of Optometry 2006 Comparison of Farnsworth and Lanthony D-15 Color Vision Tests to an Computerized Color Vision Cap Rearrangement Test James Kundart Pacific nU iversity Karl Citek Pacific nU iversity Follow this and additional works at: http://commons.pacificu.edu/coofac Part of the Optometry Commons Recommended Citation Kundart, James and Citek, Karl, "Comparison of Farnsworth and Lanthony D-15 Color Vision Tests to an Computerized Color Vision Cap Rearrangement Test" (2006). Faculty Scholarship (COO). Paper 27. http://commons.pacificu.edu/coofac/27 This Poster is brought to you for free and open access by the College of Optometry at CommonKnowledge. It has been accepted for inclusion in Faculty Scholarship (COO) by an authorized administrator of CommonKnowledge. For more information, please contact [email protected]. Comparison of Farnsworth and Lanthony D-15 Color Vision Tests to an Computerized Color Vision Cap Rearrangement Test Description Inherited color vision deficiency affects approximately 8% of the male Caucasian population, 5% of non- Caucasian males, and 0.4% of all women. In addition, significant numbers of patients of both genders acquire color vision loss due to ocular disease or pharmaceutical medications. Yet in many clinical settings color vision testing presents a challenge because plate tests, like those designed by Ishihara, do not easily differentiate green (deutan) from red (protan) defects. Tests that do differentiate, like the Farnsworth D-15, show false positive results with mild to moderate anomalous trichromacy, and are time- consuming. -
A Bilateral Color Anomaly in the Crayfish, Orconectes Immunis (Hagen)
Proceedings of the Iowa Academy of Science Volume 76 Annual Issue Article 64 1969 A Bilateral Color Anomaly in the Crayfish, Orconectes immunis (Hagen) Virgil E. Dowell University of Northern Iowa Leonard P. Winier University of Northern Iowa Let us know how access to this document benefits ouy Copyright ©1969 Iowa Academy of Science, Inc. Follow this and additional works at: https://scholarworks.uni.edu/pias Recommended Citation Dowell, Virgil E. and Winier, Leonard P. (1969) "A Bilateral Color Anomaly in the Crayfish, Orconectes immunis (Hagen)," Proceedings of the Iowa Academy of Science, 76(1), 487-492. Available at: https://scholarworks.uni.edu/pias/vol76/iss1/64 This Research is brought to you for free and open access by the Iowa Academy of Science at UNI ScholarWorks. It has been accepted for inclusion in Proceedings of the Iowa Academy of Science by an authorized editor of UNI ScholarWorks. For more information, please contact [email protected]. Dowell and Winier: A Bilateral Color Anomaly in the Crayfish, Orconectes immunis (Ha A Bilateral Color Anomaly in the Crayfish, Orconectes immunis (Hagen) VIRGIL E. DOWELL AND LEONARD P. WINIER1 Abstract. A live female crayfish; Orconectes immunis (Hagen) exhibit ing unusual body coloration was given to the biology laboratories at the University of Northern Iowa for study. Its right half, including antennae and other appendages, was colored an azure blue; the left half was colored normally. This bilateral coloration mosaicism persisted foUowing molting. Gynandromorphism as a corollary factor is eliminated on the basis that no apparent external sexual intergradation of sexual dimorphism was notice able. -
Light and Color
CS148: Introduction to Computer Graphics and Imaging Light and Color Painting by Cheryl Yaney Topics Physics of light Electromagnetic spectrum Fundamental operations: add, filter, measure Perception of color Trichromatic theory Luminance Color spaces Art Color terms Color wheels and intuitive color spaces CS148 Lecture 10 Pat Hanrahan, Winter 2009 Page 1 Physics of Light Light Image from Clive Maxfield CS148 Lecture 10 Pat Hanrahan, Winter 2009 Page 2 Electromagnetic Spectrum Image from Clive Maxfield CS148 Lecture 10 Pat Hanrahan, Winter 2009 Sources Visible (300-800 nm) spectra power distribution CS148 Lecture 10 Pat Hanrahan, Winter 2009 Page 3 Sources Visible (300 – 800 nm) spectra power distribution CS148 Lecture 10 Pat Hanrahan, Winter 2009 Adding Light Energy CS148 Lecture 10 Pat Hanrahan, Winter 2009 Page 4 Reflecting Light CS148 Lecture 10 Pat Hanrahan, Winter 2009 Light Operations Add spectra Multiply spectra CS148 Lecture 10 Pat Hanrahan, Winter 2009 Page 5 Measuring Light Photon detector CS148 Lecture 10 Pat Hanrahan, Winter 2009 Perception of Color Page 6 Color Matching Adjust brightness of three primaries to “match” color C – color to be matched Lasers: R = 700 nm, G = 546 nm, B = 435 nm C R G B C = R + G + B Result: all colors can be matched with three colors Therefore: humans have trichromatic color vision CS148 Lecture 10 Pat Hanrahan, Winter 2009 RGB Color CS148 Lecture 10 Pat Hanrahan, Winter 2009 Page 7 Human Retina: Three Types of Cones From http://webvision.med.utah.edu/imageswv/fovmoswv.jpeg CS148 Lecture -
Chromagen Lenses and Abnormal Colour Perception
S Afr Optom 2011 70(2) 69-74 Chromagen lenses and abnormal colour perception O Matthew Oriowo* and Abdullah Z Alotaibi† *Department of Optometry, Faculty of Health Sciences, University of Limpopo, Turfloop Campus, Private Bag X1106 Sovenga, 0727 South Africa †Department of Optometry, College of Applied Medical Sciences, King Saud University, PO Box 10219, Riyadh, 11433 Saudi Arabia < [email protected]> Received 26 October 2010; revised version accepted 16 May 2011 Abstract pants comprised two subjects with protanomaly, two with protanopia, five with deuteranomaly, and Background: The Chromagen lens system compris- two with deuteranopia. Amongst the two female es of tinted spectacle or contact lenses, each with a participants, one subject showed deuteranomaly, specific colour wavelength filter which controls the and one showed protanomaly. Different types of spectra of the light entering the eye. This study in- Chromagen spectacle lenses displayed some lev- vestigated whether spectacle-mounted Chromagen els of colour vision enhancement depending on lenses would enhance colour perception in individ- type of CVD. uals with abnormal colour vision. Conclusion: The findings support the notion that Methods: The Ishihara colour test was used to chromagen lenses could enhance colour vision test for colour vision deficiency (CVD) and also perception in some cases of red-green colour vi- to evaluate the effect of the Chromagen spectacle sion defects. Clients with CVD should be man- lens on colour perception in 13 subjects. An Oculus aged on an individual case basis. (S Afr Optom Anomaloscope was used to confirm and sub-classi- 2011 70(2) 69-74) fy the types of CVD. -
Optopad for Detection of CVD Dolores De Fez M
NEW IPAD-BASED TEST FOR THE DETECTION OF COLOUR VISION DEFICIENCIES Running title: Optopad for detection of CVD Dolores de Fez1 Mª José Luque2 Lucía Matea1 David P. Piñero1,3 Vicente J. Camps1 1Department of Optics, Pharmacology and Anatomy, University of Alicante, Spain 2Department of Optics, University of Valencia, Spain 3Department of Ophthalmology (Oftalmar), Vithas Medimar International Hospital, Alicante, Spain Corresponding author: Dolores de Fez, [email protected] 1 ACKNOWLEDGEMENTS The authors acknowledge the support of FUNCAVIS (Foundation for the Visual Quality, Alicante, Spain) for allowing participating in their lazy eye screening campaign in different schools by including the assessment of the colour vision with the Optopad test. 2 ABSTRACT Purpose: To develop and validate a new iPad-based colour vision test (Optopad). Methods: A total of 341 student eyes were enrolled in a first comparative study between Optopad and the Isihara tests. In a second comparative study, Optopad vs. the Farnworth-Munsell test (FM 100H), a total of 66 adult eyes were included. Besides the agreement between tests, the correlation between FM 100H and Optopad outcomes were investigated. Multiple regression analysis was used to predict the Total Error Score (TES) from contrast thresholds measured with the Optopad test. Results: The Ishihara and Optopad tests detected the same anomalous patients. Concerning FM 100H vs. Optopad, 10 subjects were diagnosed as anomalous with both tests, 3 mild anomalous cases based on TES were classified as normal with Optopad, and 2 anomalous subjects based on Optopad test showed normal TES values. Statistically significant correlations of TES and partial error red-green (PTESRG) with thresholds measured with the red-green Optopad stimuli were found.