Preview

Genetic Testing Persuasive Essay

Good Essays
Open Document
Open Document
554 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Genetic Testing Persuasive Essay
Adolescents should be allowed to partake in predictive or predispositional genetic testing without discouragement from medical facilities or family members. Huntington’s disease is an inherited disorder that arises from a mutation in the HTT gene, which codes for the huntingtin protein. The disease presents fatal complications because it causes degeneration of nerve cells in the brain, which in turn negatively impacts physical and mental performance (Mayoclinic). Symptoms of the disease include muscle control problems, personality changes, reduced memory, loss of impulse control, and depression.
There are many components to a genetic test for Huntington’s disease. Firstly, prior to taking a genetic test for Huntington’s disease, a person must undergo a process that consists of genetic counseling, a neurological examination, and a psychological interview (Huntington’s Outreach Program for Education at Stanford). Genetic counseling allows adolescents to better comprehend their decision of undergoing a genetic test by explaining the disadvantages as well as benefits of knowing their medical futures (National Society of Genetic Counselors). Genetic testing for Huntington’s disease
…show more content…
First everyone opting to take a genetic test for Huntington’s Disease must undergo the preliminary steps mentioned above. This prepares the adolescent for any outcome of the genetic test, and provides them with the time and information necessary to making a final decision about taking it. The neurological examination can determine the most likely outcome of the test through an analysis of any symptoms that the adolescent is already showing signs of. If genetic testing confirms Huntington’s Disease, the adolescent will be more aware with what is happening to their body and

You May Also Find These Documents Helpful

  • Good Essays

    One major ethical issue that surrounds Huntington’s disease concerns the genetic test that is used to diagnose the disease.…

    • 125 Words
    • 1 Page
    Good Essays
  • Satisfactory Essays

    Huntington’s disease is inherited as a dominant gene, because it is passed on with each generation.…

    • 468 Words
    • 2 Pages
    Satisfactory Essays
  • Better Essays

    The condition is diagnosed through genetic testing. It is specifically DNA-based methylation testing to distinguish the absence of the paternal chromosome; chromosome 15.This test is recommended for new borns with pronounced hypotonia (praderwillisyndrome, 2010). An early diagnosis allows for early intervention as well as early provision of growth hormone (GH) treatment. GH gives an increased muscle mass and supports linear growth. GH…

    • 2227 Words
    • 9 Pages
    Better Essays
  • Good Essays

    The Human Genome project, a revolutionary study that spanned over 13 years, hoped to discover more about the DNA of humans. The study's main goal was to provide new information to help with the diagnosis, treatment and prevention of genetic disorders. From the substantial amount of information and knowledge acquired from the project, new ways to test for genetic disorders, and the probabilities of inheriting disorders was gained. Gene testing, which involved taking a sample of a persons DNA, helped screen for a number of different disorders and problems. Before genetic testing, couples at risk of conceiving a child with a particular genetic disorder would have to initiate the pregnancy and then undergo the testing, faced with the dilemma of terminating the birth if the results weren't good. But because of the new technology available, with the combined effort of IVF, sperm and egg cells can be removed from both individuals, and the eggs would then be fertilized within a laboratory. The embryo's would then be tested for genetic mutations,…

    • 701 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Purpose: This assignment is to help you gain insight regarding the influence of genetics on an individual’s health and risk for disease. You are to obtain a family genetic history on a willing, non-related, adult participant.…

    • 1153 Words
    • 5 Pages
    Good Essays
  • Good Essays

    In 1995, genetically 50% out of 1,000 people in the population end up or effected by Huntington’s disease. (Phillips, Dennis H.) Huntington’s disease commonly known as HD is an inherited disease that causes certain nerve cells in the brain to waste away.(National Library of Medicine) This basically means that you lose all function of what might seem like the most simplest thing to do like walking and talking. Even raising your hand will be almost impossible to do with Huntington’s disease. This disease usually takes over your body at the ages between 30 or 40. If you get it before the age of 20 it is now called Juvenile Huntington’s disease (national liberty of medicine).…

    • 1057 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Genetic testing has potential benefits, such as you can see if your chromosomes are positive for a genetic mutation. Test results can provide a sense of relief from uncertainty about having a mentally or physical ill child because no one wants that for your child. They also help people make informed decisions about managing their health care. For example, a negative result for the mutation can eliminate the need for unnecessary checkups and screening tests in some cases. A positive result, having the mutation, can direct a person toward available prevention, monitoring, and treatment options. Some test results can also help people make decisions about having children. Newborn screening can identify genetic disorders early in life so treatment can be started as early as possible.…

    • 632 Words
    • 3 Pages
    Good Essays
  • Better Essays

    The defective gene codes the blueprint for a protein called huntingtin. This protein's normal function isn't yet known, but it's called "huntingtin" because scientists identified its defective form as the cause of Huntington's disease. Defective huntingtin protein leads to brain changes that cause abnormal involuntary movements, a severe decline in thinking and reasoning skills, and irritability, depression and other mood changes.…

    • 3394 Words
    • 12 Pages
    Better Essays
  • Powerful Essays

    This final paper will discuss the ongoing debate of genetic/prenatal testing. Procedures for genetic/prenatal testing have been available since the early 1970's (Press, 2008, pp. 73-78). Genetic testing identifies abnormalities or changes in the chromosomes and genes. This type of testing is used to confirm or deny a suspected genetic condition or used to predict a person's chances of developing or passing on a certain disorder (Grant, 2000). Once the woman wants to go ahead with the genetic testing, a primary care doctor or genetic specialist places an order for the test. Genetic testing is often done as part of a genetic consultation (Press, 2008, pp. 73-78). It is very important that the patient knows every aspect of the procedure including…

    • 1673 Words
    • 7 Pages
    Powerful Essays
  • Good Essays

    Genetic testing to look for defects in the genes that are linked with the disease…

    • 733 Words
    • 3 Pages
    Good Essays
  • Better Essays

    Although characterized as an “adult on-set” disease, it can affect children as well (Medterms, 1998). Huntington’s is a genetic disorder that main affects people in their 40’s and 50’s (Team C, 2011). I mainly affects the brain which leads to a gradual loss of control of movement along with memory loss and a loss of mental ability (Team C, 2011). I suppose you could say it is essentially a breakdown of the brain and the functions that are accompanied with it (Team C, 2011). With Huntington’s disease comes certain personality changes and depression along with some other mental illnesses (Team C, 2011). As of now there is no known cure but there have been a few case studies researching the possibility of a cure (Team C, 2011). Huntington’s disease has a pattern known as “autosomal dominance” (Team C, 2011). Autosomes Are the chromosomes inside the cells of the body aside from the sex chromosomes (Team C, 2011). This is where our body’s genetic information is stored and located (Team C, 2011). The genetic abnormality that is normally associated with Huntington’s disease is located on the fourth chromosome and the three bases arranged along the chromosome happen in a repeated sequence (Team C, 2011). An excess amount of the repeats leads to Huntington’s disease (Team C, 2011). Any more than 35 reps of this particular sequence is often attributed to Huntington’s but…

    • 1220 Words
    • 5 Pages
    Better Essays
  • Good Essays

    From a patient’s perspective, people tend to see genetic information as more definitive, in the sense that 'you cannot change your genes' and that 'genes tell all about your future.’ Such genetic determinism is an oversimplification and does not take into account the nature of biologic pathways. From a provider’s perspective, genomics presents challenges with respect to ethical and professional responsibilities, including the appropriate use of genomic information in the health care setting. I believe that there should be an identification of provider education programs that increase use of appropriate screening, counseling and evidence-based genetic tests. By increasing the effectiveness of genomic testing, it will help dissolve the negative association and further increase the proportion of people who are willing to receive genetic…

    • 463 Words
    • 2 Pages
    Good Essays
  • Good Essays

    As research continues to uncover new disease-causing mutations, the prospect of stopping the transmission of heritable diseases increases. With the use of modern technology, expecting parents can now be prescreened in order to determine their carrier status for certain diseases. Parents who choose to use in vitro fertilization are able to choose embryos that are free of disease due to preimplantation genetic diagnosis. Additionally, parents can be provided with information on their unborn child with the use of prenatal genetic testing. Some individuals view modern genetic technology as eugenic; however, this biggest difference between eugenics now and eugenics during the 1900s is consent. Today individuals pursue genetic testing by choice and policies on ethics and consent prevent reoccurrences of the immoral endeavors within the field of…

    • 585 Words
    • 3 Pages
    Good Essays
  • Good Essays

    The gene that carries the mutation for Huntington’s disease follows a heterozygous dominant line of inheritance. This…

    • 1026 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Though there are tests and testing facilities that do the genetic tests, prenatal genetic testing is not accessible to all at-risk or concerned families expecting a baby. Government funding should be put towards prenatal genetic testing to increase accessibility to testing facilities, discover more testing forms, and give more autonomy to physicians. With these improvements, low income-families and anyone with a family history of genetic diseases can find out and prepare for any irregularities before the baby is…

    • 846 Words
    • 4 Pages
    Good Essays