scholarly journals ANIMASI INTERAKTIF SIMULASI TES BUTA WARNA DENGAN METODE ISHIHARA BERBASIS ADOBE FLASH CS 5

Petir ◽  
2018 ◽  
Vol 10 (2) ◽  
pp. 29-36
Author(s):  
Redaksi Tim Jurnal
Keyword(s):  
Genetic Factors ◽  
Genetic Disorder ◽  
Color Blindness ◽  
Blind Test ◽  
Adobe Flash ◽  
Lack Of Information ◽  
Cone Cells ◽  
Color Spectrum ◽  
Colour Blindness ◽  
Color Blind

Colour blindness isi disorder caused by the inability of teh eys cone cells to capture a spesific color spectrum due to genetic factors. Color blindness is a genetic disorder/ congenital inherited from parents to their childern, because this disorder is carried by the X chomeosome. Many people find out too late in the color blindness.This isi due to lack of information and insight about the color blind test. Therefore, this aplication is made so that people can find out about all sort of color blindness test, the results of each simulation to make simulation aktratif silmulation is made with adobe cs 5

scholarly journals Prevalence of Phenylthiocarbamide (PTC) Taste Sensitivity and Colour Blindness in Tengger Tribe Population, Ranupani Village, Senduro, Lumajang

2021 ◽  
Vol 9 (4) ◽  
pp. 174
Author(s):  
Rike Oktarianti ◽  
Iguh Widigda Putra ◽  
Resmining Mega Arofa ◽  
Asmoro Lelono
Keyword(s):  
Allele Frequency ◽  
Autosomal Dominant ◽  
Color Blindness ◽  
Pedigree Analysis ◽  
Dominant Trait ◽  
Genetic Trait ◽  
Autosomal Dominant Trait ◽  
Colour Blindness ◽  
Color Blind

The taste of sensitivity of phenylthiocarbamide (PTC), is autosomal dominant trait inherited while the colour blindness is a sex linked genetic trait on the X chromosome. The purpose of this study was to determine the distribution of taster and non taster phenotypes, prevalence of color blindness, frequency of taster and non taster alleles, and frequency of color blind alleles, as well as pedigree analysis in non taster and color blind families. The research was conducted on the Tengger tribe, in Ranupani village, Senduro, Lumajang. Determination of the sample is carryout randomly. Detection of the ability to taste PTC was respondents to taste the PTC solution from the lowest concentration of 0.32mg/L (P13) to the highest concentration of 1300 mg/L (P1). Color blindness detection by the Ishihara method. The results of the study showed that the distribution of the taster was 98.1% while the non-taster was 1.9%. The allele frequency of the dominant taster (T) was 0.86 and the recessive allele non taster (t) is 0.14. The prevalence of color blindness in the population of the Tengger tribe was 0.63% and the allele frequency for color blindness was 0.013. The pedigree analysis of non taster family showed that non taster individuals were born from taster couple (Tt) or from couple of non taster (tt) with tasters (Tt) heterozigot. While the pattern of inheritance of color blindness was criss-cross inheritance pattern, which is passed from mother to son.

Color Blind Test Using Ishihara Method for Mercu Buana University Prospective Students Selection

2021 ◽  
Vol 9 (2) ◽  
pp. 135-146
Author(s):  
Sri Dianing Asri ◽  
Adhitya Dwiki Darmawan ◽  
Novianti Putri Wibowo ◽  
Dimas Riyanto Wibowo
Keyword(s):  
System Development ◽  
Test Procedure ◽  
Color Blindness ◽  
Test Results ◽  
Prospective Students ◽  
Blind Test ◽  
Vision Disorder ◽  
Test Application ◽  
New Students ◽  
Color Blind

Mercu Buana University is a private university which consists of seven faculties. At the Faculty of Design and Creative Arts, Faculty of Communication Sciences and Faculty of Engineering, additional requirements are required for new student candidates, i.e. a color blindness free certificate. Color blindness is a vision disorder caused by the inability of the eye cone cells to perceive a certain spectrum of colors. There are many ways to test someone's color blindness, one of which is by using the Ishihara method. To obtain a color blindness free certificate, prospective students must visit a clinic or hospital, carry out the applicable color blind test procedure, then bring the results to campus. Based on these problems, the research was conducted with the aim of making a color blind test application that can issue a recommendation letter based on the test results of prospective new students. The system development method uses  System Development Life Cycle. The results of the study were an android-based color blind test application that was able to detect color blindness using the Ishihara method and issued a recommendation letter based on the test results of prospective new students in the on-time application.

scholarly journals Building Systems Testing Method Using Ishihara Color Blindness

2020 ◽  
Vol 2 (2) ◽  
pp. 218-221
Author(s):  
Faduhusi Lombu ◽  
Erwin Panggabean
Keyword(s):  
Color Blindness ◽  
Test System ◽  
Prospective Students ◽  
Blind Test ◽  
Driver's License ◽  
Computer Based ◽  
Color Blind ◽  
Global Futures ◽  
Crystal Report ◽  
Test Requirements

Color blind test system is needed in various needs such as the management of a driver's license, prospective students in Certain institutions, prospective employees or employees in government and private agencies. The development of a computer-based test system color blind color blind tests aims at activities that produce normal eye Conclusions on sealing, partial color blindness and total color blindness. The method used to complete this research is Ishihara, which was discovered by Dr. Shinobu Ishihara. For the construction of the Ishihara color-blind method of testing using the stages of analysis, design and implementation. The developed test system aims to be used as a color blind tests for the health test requirements as a requirement for prospective employees at PT JAVA GLOBAL FUTURES Medan. To build this color blind test system used MS-Visual Studio 2010 and the results were made using Crystal Report 2010. This research has produced a Color Blind Test System with the Ishihara roomates Computer Based Method is used for the color blind tests at PT JAVA GLOBAL FUTURES Medan. With the output in the form of computer screens and paper prints when using a printer connected to a computer in the form of a Health Certificate with test results in the form of a normal eye vision, color blindness partial or total color blindness.

scholarly journals Pembuatan Aplikasi Buta warna untuk penderita buta warna

2019 ◽  
Vol 10 (2) ◽  
pp. 42
Author(s):  
Adi Hartanto ◽  
Nur Ismawati
Keyword(s):  
Color Blindness ◽  
Color Correction ◽  
Android Os ◽  
Cone Cells ◽  
Color Blind ◽  
Retinal Cone

Color blindness is the reason a person is unable to distinguish certain colors. Color blindness is experienced by someone from birth because of lack or absence of pigment in the retinal cone cells of the eye. So that someone will be difficult to distinguish and identify colors. The purpose of making this color-blind application is to help people with color blindness and know the color by making color transfusion and color correction to display names, RGB and HSV values of a color. This Color Blind application is an Android OS application that will be embedded in a smartphone that can be easily used by people with color blindness

PERANCANGAN PROGRAM APLIKASI TES BUTA WARNA BERBASIS ANDROID

2019 ◽  
Vol 2 (1) ◽  
pp. 1-19
Author(s):  
Tedi Budiman
Keyword(s):  
Color Blindness ◽  
West Java ◽  
Blind Test ◽  
Circle Pattern ◽  
Test Application ◽  
Health Agencies ◽  
Long Time ◽  
Color Blind ◽  
The Right ◽  
Lack Of Knowledge

Color blindness test is one way to find out whether a person has color blindness or not, is usually done with the Ishihara method. This Ishihara method is a method where when running a test with this method, the patient is usually faced with a book containing a circle pattern (disk) with many points of various colors and sizes in it. The circle pattern is usually 14, 24 and 38 dishes. Tests like this are usually done in health agencies, one of which is the Cahaya Insani Clinic in Garut, West Java. The process of implementing a color-blind test is still done manually where people who want to do a color-blind test must come directly to the clinic, making people who did color-blind tests had to be willing to wait a long time to be able to do a color-blind test. In addition to these problems, the lack of knowledge and understanding of the community regarding color blindness, makes people less aware of the importance of color-blinding tests early on. Therefore, a media is needed that can do color blindness tests quickly and easily, coupled with information about color blindness that can provide insight to the community. Mobile based application Android is one of the right media to make it easy for people to obtain information. Starting from this, then made an Android-based color blindness test application to make it easier for people to do color blindness tests anytime and anywhere, and can used as a medium of information about color blindness.

Color Blindness in Mentally Retarded Children

1969 ◽  
Vol 35 (8) ◽  
pp. 609-616 ◽  
Author(s):  
Jerome D. Schein ◽  
John A. Salvia
Keyword(s):  
Sex Differences ◽  
General Population ◽  
Color Vision ◽  
Mentally Retarded ◽  
Color Blindness ◽  
Instructional Materials ◽  
Normal Children ◽  
Color Blind ◽  
Mentally Retarded Children

Recent studies of mentally retarded children have found substantially higher rates of color blindness than are usually reported for the general population. In 2 of these studies, sex differences in color blindness, invariably found in intellectually normal children, do not appear. Reanalysis of data from one of the studies of retarded children suggests the possibility that the high rates arise from the difficulty in comprehending the test and following the directions rather than from faulty color vision. However, even if the number of color blind retarded children is actually lower than these studies show, the need for research on this topic seems apparent. Using color dependent instructional materials with color blind, mentally retarded children may be detrimental.

scholarly journals Do Color Blindness and Multiculturalism Remedy or Foster Discrimination and Racism?

2018 ◽  
Vol 27 (3) ◽  
pp. 200-206 ◽  
Author(s):  
Victoria C. Plaut ◽  
Kecia M. Thomas ◽  
Kyneshawau Hurd ◽  
Celina A. Romano
Keyword(s):  
Color Blindness ◽  
People Of Color ◽  
Organizational Diversity ◽  
Interracial Interactions ◽  
Organizational Contexts ◽  
Psychological Science ◽  
Diversity And Inclusion ◽  
Color Blind

This article offers insight from psychological science into whether models of diversity (e.g., color blindness and multiculturalism) remedy or foster discrimination and racism. First, we focus on implications of a color-blind model. Here, the literature suggests that while color blindness appeals to some individuals, it can decrease individuals’ sensitivity to racism and discrimination. Furthermore, the literature suggests that, with some exceptions, color blindness has negative implications for interracial interactions, minorities’ perceptions and outcomes, and the pursuit of diversity and inclusion in organizational contexts. Second, we examine circumstances under which a multicultural approach yields positive or negative implications for interracial interactions, organizational diversity efforts, and discrimination. The research reviewed coalesces to suggest that while multiculturalism generally has more positive implications for people of color, both models have the potential to further inequality.

scholarly journals GENETIC DISORDER ALZHEIMER

2017 ◽  
Vol 10 (12) ◽  
pp. 36
Author(s):  
Pratibha Rani ◽  
Kamaldeep Singh ◽  
Anania Arjuna ◽  
Savita Devi
Keyword(s):  
Genetic Factors ◽  
Metabolic Diseases ◽  
Genetic Disorder ◽  
Memory Loss ◽  
Amyloid Plaque ◽  
Specific Protein ◽  
Inhibitor Molecule ◽  
Common Sign ◽  
A Chain ◽  
The Brain

Alzheimer’s disease (AD), slowly continuous neurological disorder, mostly appears in older >65 age that deals with the memory loss due to death or damage of brain cells and cognitive functions (thinking, reasoning, and behavior abnormalities) due to the accumulation of the specific protein (beta-amyloid protein) which form plaque and fibers (tau tangles) in the brain. Not only the genetic factors are responsible but also most of the non-genetic factors are responsible for AD. Several mutations in the gene (APP, APOE, PENS1, PENS2 on chromosome no. 21, 19, 14, 1) are responsible for causing four types of AD. Memory loss is most common sign of AD. Predisposing factors of AD are hereditary, severe brain injury or traumatic, and metabolic diseases such as diabetes mellitus, hypercholesteremia, and obesity. Although treatment can manage some symptoms in few people, but there is no current mechanism to cure AD or stop its progression. Beta-secretase inhibitor molecule prevents the first step in a chain accumulation which leads to the formation of amyloid plaque in the brain. However, the scientist or researchers have established a compound NIC5-15 they have been found NIC5-15 has safe and effectual treatment which has been used to stabilize cognitive performance in patients with mild to moderate AD.

scholarly journals Color-Blind Racism in Pandemic Times

2020 ◽  
pp. 233264922094102
Author(s):  
Eduardo Bonilla-Silva
Keyword(s):  
Popular Culture ◽  
Color Blindness ◽  
Differential Mortality ◽  
Main Argument ◽  
Government Officials ◽  
Structural Nature ◽  
Color Blind Racism ◽  
Color Blind ◽  
Tv Shows ◽  
Magazine Articles

In this article the author examines how the frameworks of color-blind racism have influenced many topics during the pandemic. Using readily available material from popular culture (TV shows, newspaper and magazine articles, and advertisements) and from statements by government officials, the author examines how color blindness has shaped our national discussion on essential workers and heroes, charity, and differential mortality. The main argument is that color-blind racism is limiting our understanding of the structural nature of the various racial problems coronavirus disease 2019 has revealed, making it difficult to envision the kinds of policies needed to address them. the author concludes by summarizing what these ideological perspectives block from view as well as addressing the nascent discursive cracks that might be used to produce alternative frames for interpreting matters and organizing collective action.

scholarly journals Harlequin ichthyosis - a rare genetic disorder : a case report

2015 ◽  
Vol 04 (04) ◽  
pp. 199-201
Author(s):  
Arnab Ghosh ◽  
B C Dutta ◽  
Sudipta Pal
Keyword(s):  
Case Report ◽  
Life Expectancy ◽  
Genetic Disease ◽  
Genetic Factors ◽  
Genetic Disorder ◽  
Treatment Protocol ◽  
Present Treatment ◽  
Harlequin Ichthyosis ◽  
Micro Anatomy ◽  
Affected Infant

AbstractHarlequin lchthyosis(HI) is a type of genodermatosis. It is a rare and fatal genetic disease. Life expectancy in an affected infant is only a few days. The defect lies in mutation of ABCA12 gene. The barrier action of skin is severely compromised making the infant prone to infections and dehydration. Present treatment protocol consists mainly of conservative and supportive therapies. The authors report this case as it is a rare disease. The main purpose of this report is to create awareness about the disease and discuss the genetic factors along with micro anatomy of skin ultimately leading to this condition.

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