Genetic testing is the analysis of human DNA, RNA, chromosomes, or proteins used to detect abnormalities related to an inherited disorder, to identify increased risks of health problems, and to assess responses or choose treatments. A person may be offered testing if they have a family history of a specific disease, have symptoms of a genetic disorder, or are worried about passing down a genetic disorder to their children. More than 1,000 genetic tests are currently in use, and many more are being developed. Depending on the type of genetic testing, they can help to diagnose disease, identify gene changes that are responsible for an already diagnosed disease, to determine the severity of a disease, to help doctors decide the best treatment to be used on a specific individual, to identify gene changes increasing the risk to develop a disease, to identify gene changes that could possibly be passed on to a child, and screen newborn babies for certain treatable conditions. They are also used for screening embryos for disease and finding genetic diseases in unborn babies. …show more content…
These can be both medical, emotional, financial, and ethical. Genetic testing may be beneficial because of the fact that it serves as a relief; as it eliminates doubt and uncertainty surrounding an individual's health. These results may help doctors make recommendations for treatment also. Overall, it helps people make informed decisions about their future, such as whether or not to have a child with the risk of passing on a genetic mutation/disease. However, the limitation of genetic testing is the fact that even though you have a positive result does not mean that you will develop the
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
Another big benefit of testing is the ability to know in advance the health of a baby. It is no longer necessary for parents to be to have to worry about the health of their child. The technology is there to know in advance. Some people have major health problems in their family. This testing could make it possible for them to give birth to healthy long living children. The whole point of prenatal genetic testing is to improve life through good health. There are enough things
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
The benefit of genetic science for individuals is that it can determine if the person has a possible genetic disorder and give them
When used in healthcare, genetic testing can show the genetic cause of a disease, confirm a suspected diagnosis of an illness, predict future illnesses, and predict responses to
Genetic testing identifies changes in ones genes and chromosomes. These changes often lead to diagnoses of conditions, disorders, or diseases. Through testing, “one can confirm or rule out a suspected genetic condition or help determine a person’s chance of developing or
In chapter four of her book Genetic Dilemmas, Dena Davis asserts that it is unethical for parents to subject their children to genetic testing for the markers of adult-onset genetic diseases because it places an unfair constraint on a child’s right to an open future. It both removes the child’s ability to choose whether to be tested as an adult and has the potential to negatively alter the overall trajectory of their lives. While the current consensus amongst medical professionals is that such testing should be prohibited (Davis, _____), many concerned parents correctly point out that discouraging such testing creates a conflict of interests between the “beneficence model of patient care and the rights of parents to their own autonomy”
Genetic testing, can affect a person’s life in many ways. Genetic testing is a type of medical testing that identifies changes that occur in chromosomes, proteins, and genes. These changes that occur can be associated, and often are associated with inherited
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
Genetic testing is normally used to determine if a person is carrying a specific mutated or altered gene which can cause a specific medical condition. JL’s parents would benefit from this because genetic testing would determine how likely it is that JL’s parents are to pass on the same mutated gene to another child. This would also determine if the mutated gene was inherited from the parents of weather or not it was a result of a random mutation.
Embryonic screening allows for the elimination of inherited diseases before birth or a treatment plan before birth. In breast cancer patients, genetic testing allows the physician to know if chemotherapy is necessary, which would expand treatment options. Genetic testing could eliminate years of experimental testing and medication use used to diagnose a new disease. Overall, genetic testing is in alignment with the core medical philosophy that early prevention leads to early treatment, which leads to an overall better outcome for the patient.
Results provided through genetic testing enables doctors to be more informed in terms of their patients; allows regular screening practices, or treatment planning at early stages.
These results may also help doctors make recommendations for treatment or monitoring, and give people more information for making decisions about their and their family's health, allowing them to take steps to lower his/her chance of developing a disease. For example, as the result of such a finding, someone could be screened earlier and more frequently for the disease and/or could make changes to health habits like diet and exercise. Such a genetic test result can lower a person's feelings of uncertainty, and this information can also help people to make informed choices about their future, such as whether to have a baby or
Probably, applied genetics' most impacts on society are as a result of genetic tests. In general, genetic tests seek to detect some feature of a person's genetic constitution. This feature can be a disease causing mutation or a marker DNA sequence used to detect presence of another gene. Obviously these procedures used for testing the status of DNA, RNA or chromosomes are included in genetic tests. What is more it is possible to include some protein based tests and classical medical examinations when they aim to detect inheritance of a trait. Genetic tests have been divided into four categories in this text, and they will be examined in greater detail later. These categories are:
genetic testing, everything has changed. She notes that clinicians now have the ability to diagnose, treat, and monitor a patient’s illnesses or disease progression in an entirely different manner. This is a far cry from the old medical model of responding to a disease (or defect) only after it appears, and then prescribing the recommended medication or intervention. These genetic medical advances sound miraculous and promising, but the ability to test, screen and provide early intervention does not come without many major ethical dilemmas.