Wait a second!
More handpicked essays just for you.
More handpicked essays just for you.
Essay paper on color blindness
Essay on color blindness
Papers on color blindness
Don’t take our word for it - see why 10 million students trust us with their essay needs.
In the Radiolab episode “Colors,” Adam Cole hosts Jay Neitz, a neurologist and color vision researcher at the University of Washington, to discuss colorblindness in primates and humans. Neitz hypothesizes that the test they used to cure colorblindness in squirrel monkeys could also cure the same disorder in humans. Colorblindness is a genetic disorder that causes the cones in the eye to perceive colors differently. In the back of the eye lies the retina that holds three photoreceptor cells called cones. Each cone is sensitive to either red, green, or blue and when functional, allows the brain to process the different wavelengths of color. Humans and some primates have two genes on the X Chromosome that encodes visual pigments, one holds green …show more content…
pigment and the other holds red (A Cure for …). When the cones are damaged, missing, or nonfunctional, their corresponding colors are unable to be processed by the eye, resulting in a misperception of that color, or colorblindness. To cure it, Neitz injected Adeno Associated Virus (AAV) with a needle into the retina of squirrel monkeys whom lacked the ability to differentiate between red and green because they only have blue and green cones (Colors 21:40-22:05). A virus is a powerful method of forcing DNA into a cell. Finding genes is simple, but contrastingly, replacing those genes inside cone cells with the correct genes is difficult (A Cure for …). Before breakfast, the monkeys take a color vision test involving a computer screen containing gray blobs and an occasional red blob. Locating the red blob allows the monkeys to receive grape-juice. Unfortunately, the morning after the injection of the red cone into the retina, the squirrel monkeys remained colorblind (Colors 22:30-23:49). It took twenty weeks for the monkeys to successfully locate the red blob. Jay Neitz mentions that after the test succeeded, some felt like the lives of the monkeys improved: he questions whether or not the monkeys’ lives improved (Colors 23:50-24:09). Whether or not the test would succeed among humans, is it ethical? If you can inject humans with the AAV in the same way as the squirrel monkeys to cure colorblindness among the red and green pigments, would it be ethical? Consequentially, having knowledge of whether or not the AAV injection is ethical would allow researchers to determine the quantity of testing and research that should continue.
Whether or not the test would succeed among humans is unknown because the test has not been conducted on any human. Legally, states biomedical engineering student at the University of Rhode Island Mary Ellen Sweeney, “in order for human testing to commence, this gene therapy and specific process must be passed, (reviewed and approved), by the NIH, ORDA/RAC, and the FDA” (Sweeney 1). However, if the AAV test is deemed ethical or not, then there does or does not exist a cure that replaces functional genes inside cone cells that eliminates colorblindness. Although, there are consequences of this treatment being ethical and that includes a bias towards test subjects who failed to see color after the injection. In addition, there would be a bias towards those who opt out of receiving the treatment. These negatives biases divide those who perceive colors correctly and those who misinterpret colors, emphasizing an anomalous error in humans with colorblindness. If the test was deemed unethical, the consequences would include a continuation of scientific research to determine a
cure. What are the To attain knowledge, the first step is to establish the proposition and identify the subject. To reiterate, the proposition present is the ethics of injecting AAV to replace the genes in the photoreceptors to correct the manner in which the retina receives color. Identifying the subject allows the proposition to be analyzed. As noted by Jennifer Nagel, professor of philosophy at the University of Toronto, “[k]nowledge demands some kind of access to a fact on the part of some living subject … Unlike water or gold, knowledge always belongs to someone” (Nagel 2). That is, having knowledge of whether or not the proposition is ethical will only be possible if some entity is present to store and accept it. Before the statement can be defined as knowledge there needs to be a media that can access it. The next step would be to define all possible outcomes on the scale of ethics. To determine how ethical the procedure is, the subjects must have a communal agreement on the definition of ethical and unethical. That is, to begin the epistemological questioning of ethics, all
The white (w) eye color gene is located on the X chromosome at 1.5 genetic map units (1). The mutation is also recessive, meaning that each fly has different copies of the gene if they are either male or female (2). In wild-type Drosophila, the brick red color is visible due to the combination of two pigments, brown and scarlet. The synthesis of drosopterin for bright red pigments is controlled by the (bw+) gene and the synthesis of ommochromes for brown pigments is controlled by the (st+) gene (7). Therefore, there are two pigment synthesis pathways that must be working in order for the flies to express the brick red eye color. In addition, transport proteins are responsible for transporting both pigments into the eye in order to express the color (8). Thus, both the pathways responsible for the synthesis of brown and red pigments must work properly as well as the genes that encode for transport proteins. Despite having white eyes, Drosophila flies with this mutation still experience normal eyesight
The experiment lasted more than forty years and did not garner media attention until 1972, when it was finally made public by Jean Heller of the Associated Press to an outraged nation. The fact that a medical practitioner would knowingly violate an individual’s rights makes one question their bioethical practices. What gives doctors the right to make a human being a lab rat? When both of these case studies began in the earlier half of the 20th century, African Americans were still fighting for the most
"Lemon Brown didn’t move. Greg felt himself near panic. The steps came closer, and still Lemon Brown didn’t move. He was an eerie sight, a bundle of rags standing at the top of the stairs, his shadow on the wall looming over him."Do to the characters decisions each one has their own up-shot. In the story, “The Treasure Of Lemon Brown,” by Walter Dean Myers, The author creates the theme, with everything their is an up-shot good or bad.
Red-green color blindness is not uncommon in the general population. The unequal crossover in the X-chromosome which causes this disorder is much more easily achieved than the mechanisms which cause other types of color blindness, due to the proximity of the two pigment genes. Five to eight percent of men are affected with this genetic condition, and due to a lacking pigment, have trouble distinguishing between red, green and brown. (1)
In September 14, 1990, an operation, which is called gene therapy, was performed successfully at the National Institutes of Health in the United States. The operation was only a temporary success because many problems have emerged since then. Gene therapy is a remedy that introduces genes to target cells and replaces defective genes in order to cure the diseases which cannot be cured by traditional medicines. Although gene therapy gives someone who is born with a genetic disease or who suffers cancer a permanent chance of being cured, it is high-risk and sometimes unethical because the failure rate is extremely high and issues like how “good” and “bad” uses of gene therapy can be distinguished still haven’t been answered satisfactorily.
Although there is no way to treat colorblindness the people who have it have never known any different; it is not that big of a deal to them. I’m sure that people with colorblindness wonder what it’s like to see color the way other people see it, but t...
Over 20 years after the proclamation of these specific ethical guidelines, we are introduced to the University of Pennsylvania’s Institute for Human Gene Therapy’s study on a delivery mechanism for gene therapy that resulted in the death of an 18 year old research subject Jesse Gelsinger. Gelsinger suffered from partial OTC (ornithine transcarbamylase) deficiency caused by a defective single gene (Obasogie, 2009).
The Human Genome Project is the largest scientific endeavor undertaken since the Manhattan Project, and, as with the Manhattan Project, the completion of the Human Genome Project has brought to surface many moral and ethical issues concerning the use of the knowledge gained from the project. Although genetic tests for certain diseases have been available for 15 years (Ridley, 1999), the completion of the Human Genome Project will certainly lead to an exponential increase in the number of genetic tests available. Therefore, before genetic testing becomes a routine part of a visit to a doctor's office, the two main questions at the heart of the controversy surrounding genetic testing must be addressed: When should genetic testing be used? And who should have access to the results of genetic tests? As I intend to show, genetic tests should only be used for treatable diseases, and individuals should have the freedom to decide who has access to their test results.
It was determined that infants develop color vision at or around three months of age and that when final results were evaluated and compared to adult (only) measures, actually have better quality color vision (Brown et al., 1994). An interesting study by Chase (1937) made efforts to discover the identities of color in which infants that aged 2 to 10 weeks old were tested to find out what colors they could perceive. The results they came up with were that very young infants could tell the difference between the primary colors and combinations but there were numerous limitations to the study (Chase, 1937). The study had placed infants to lie down and view a screen while observing eye movements (Chase, 1937). Findings by Franklin, Pilling, and Davies (2005) explain that color categorizing occurs in four month old infants and adults alike. A study by Bornstein, Kessen, & Weiskopf (1976) has supporting evidence that color is categorized in 4 month old infants and determined the boundaries within...
Allen, B., (1994). Predictive genetic testing: ethical, legal and social implications. USA Today Nov 1994:66-69. Reference 2.
In today’s world, people are learning a great deal in the rapidly growing and developing fields of science and technology. Almost each day, an individual can see or hear about new discoveries and advances in these fields of study. One science that is rapidly progressing is genetic testing; a valuable science that promotes prevention efforts for genetically susceptible people and provides new strategies for disease management. Unnaturally, and morally wrong, genetic testing is a controversial science that manipulates human ethics. Although genetic testing has enormous advantages, the uncertainties of genetic testing will depreciate our quality of life, and thereby result in psychological burden, discrimination, and abortion.
High profile adverse events resulting in disproportionate media attention have prevented a greater difficulty for the field, with the death of Jesse Gelsinger in a trial of gene therapy for ornithine transcarbamylase deficiency undermining public trust of clinical research in the US. There is a danger that the gene therapy field may have become too risk-averse in response to these adverse events, and that this could manifest as fewer trials that take longer to commence. In the context of a research environment that is increasingly turning to the developing world for the expedient conduct of clinical trials, it is imper...
The background setting of most of Chopin's stories is the Creole culture of southern Louisiana. Southern Louisiana was far more French than American as a large portion of the culture was Creole -- those being the descendants of French and Spanish colonists.
The images formed on the two retinas are so unlike that they cannot be blended in the brain. Thus, a double image is perceived. The condition is known as diplopia, or double vision. Prismatic lenses are prescribed to correct this defect.Imperfections in the cones of the retina, resulting from heredity or disease, cause defective color vision. This is known as color blindness, or Daltonism. In total color blindness, everything appears in shades of gray.