Case Study: Cracking Your Genetic Code

Presume a couple found out their embryo has a gene mutation that has a high success rate of causing cancer later on in the baby's life. Would you advocate the use of gene therapy in the embryo to correct the problem before the child was ever born?

Genetic testing is a medical test of one’s DNA that identifies changes in chromosomes, genes, or proteins. The results of a genetic test can confirm or rule out a suspected genetic condition which can help determine an individual's chance of developing or passing on a genetic disorder. In addition, knowing one’s genetic code can help individuals improve their wellness, prevent the onset of diseases they are at risk for, or lessen the harmfulness of diseases they do contract. NOVA’s documentary on PBS, “Cracking Your Genetic Code” demonstrates what exactly genetic testing is, how genetic testing is performed, and in addition the film showed stories about some individuals that have benefited from these special DNA techniques. The film plot focuses

The view over genetic testing starts with establishing necessary definitions and discussing its purpose in our world. To start off, the human body is a complex multicellular system. Every cell in the body is comprised of the same DNA (with some exceptions), which stores our genes. These genes are the set of instructions that encode the proteins necessary to create and maintain the human body. The issue is that some genes can undergo a variety of mutations during development that cause an array of complications or disease. Gene therapy can modify the designated abnormal genes to reach normalcy, while genetic engineering focuses on enhancement and surpassing what is normal. However, the goal of genetic testing is to identify the abnormalities

Children born today have a fifty-fifty chance to live to be one hundred years old or more, and the quality of their lives will be affected by the research and empirical data that is being generated by organizations dedicated to helping developmentally disabled adults live more meaningful lives. These programs also serve as a benchmark in the battle against cerebral palsy in general and provide valuable best practice examples, thereby influencing the American health care system as a whole. While the search for a cure continues, cerebral palsy represents a debilitating disease that can adversely affect the ability of sufferers to provide for the basic needs of living, but with appropriate treatment and care, many are able to accomplish far more than most observers might believe in terms of their independence, productivity and integration with larger American society, goals that are also legally mandated. To determine how these positive clinical outcomes are possible, this paper provides a review of the relevant peer-reviewed and scholarly literature concerning the role of United Cerebral Palsy in delivering high quality care pursuant to the Developmental Disabilities Assistance and Bill of Rights Act of 2000 as overseen by the U.S. Department of Health and Human Services to determine the effect of this oversight on a representative

All women should be offered genetic testing during child-bearing years. It may be done before pregnancy or during pregnancy.

What level of prenatal genetic testing for abnormalities acts with beneficence to the patient, and what level of trait selection is ethical?

As you can see genetic testing is very important and can affect a child's and parents lives for the better and the worst. Children all over the world have serious genetic diseases that affect their life on a daily. Some of these diseases are Achondroplasia, Down syndrome, and Turner's syndrome. Many believe genetic testing is a good way to test for these genetic conditions before the child is even born, but others think that it can harm the baby very badly and even cause a miscarriage, so they choose not to do this kind of testing. Knowing about the most serious genetic diseases is very important for expecting parents to be informed as well as being

If rejecting an “undesired” embryo means preventing the genetic inheritance of a seriously debilitating disease, then maybe some benefit can be achieved for the greater good of human kind. However, I do not feel there is any benefit in screening embryos for desired traits, and rejecting the “undesired” embryos for superficial or cosmetic reasons. For example, I would not agree with a person screening embryos to create their epiphany of a beautiful baby.

The medical advances being made feasible by genetic testing are very exciting. It is possible for people with predispositions for genetic defects to know in advance if they will have a healthy child or not. If they find out there is a problem they can choose to terminate the pregnancy or they can prepare in advance for their child's special needs. There is even new technology called Ex Utero genetic testing. This test is performed on eggs fertilized through in vitro fertilization before they are even put in the mother's uterus. Understanding genes in the developing human will help doctors understand the nature of genetic diseases and may lead to countless other medical breakthroughs. Though it is probably a long way off doctors may one day be able to manipulate genes. If this is possible some genetic problems may be cured.

   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

One of the benefits of prenatal screening is to enable early detection of the developmental defect embryology. This embryology developmental defect may be due to the mutation or genetic inheritance. Mutation is a condition characterized by permanent change in the DNA sequence that makes up a gene. It can range in different sizes from a single DNA building block (DNA base) to a large segment of a chromosome. On the other hand, genetic inheritance is a condition whereby parents pass traits such as height and other characteristics to the children by chromosomes. “Sonograms, genetic tests and a new test called pre-implantation genetic diagnosis -- which is a genetic test conducted on embryos for people attempting pregnancy through in vitro fertilization -- allow women to better predict if the infant will have a genetic defect” (New York Times Magazine, 2006). Thus thorough these tests, medical practitioners are able to identify and make early preparation toward any abnormalities of the fetus.

Genetic engineering has been around for many years and is widely used all over the planet. Many people don’t realize that genetic engineering is part of their daily lives and diet. Today, almost 70 percent of processed foods from a grocery store were genetically engineered. Genetic engineering can be in plants, foods, animals, and even humans. Although debates about genetic engineering still exist, many people have accepted due to the health benefits of gene therapy. The lack of knowledge has always tricked people because they only focused on the negative perspective of genetic engineering and not the positive perspective. In this paper, I will be talking about how Genetic engineering is connected to Brave New World, how the history of

Cerebral palsy cannot be cured although early support and therapeutic intervention can help children’s development.

Cerebral palsy is a brain and nervous system disorder that was discovered in the mid nineteenth century by a group of people with a generous commitment of improving the lives of people with disability (MyChildatCerebralpalsy.org, 2014). One of such individuals is William Little, who pioneered customary studies relating to cerebral palsy by using his childhood disability to substantiate the causal relationships between natal complications and physical and

I think that everybody should do a genetic test at a very early age in order to know what is going on with their genes. Even if a genetic test is positive, a genetic counselor, doctor, or other health care professional trained in genetics can help an individual or family understand their test results. These professionals can also help explain the incidental findings that a test may yield, such as a genetic risk factor for a disease that is unrelated to the reason for administering the test, so they can clarify the implications of test results for other family members. Doing a genetic test is crucial because on an expanded panel, certain cancer can be entirely reversed with an early intervention like dietary