Anyone could be a carrier of a genetic disorder. What do you think could help them if they are at risk, what do they do? Do they not have children? Are they going to have to worry about their children getting the same disorder that may be in there own DNA? These are some of the questions for thousands of people around the world for people who have disorders. “Genetic Screening is the process of testing DNA to determine a person’s risk of having or passing on a genetic disorder.” Because our knowledge is still limited, it’s not yet possible to test for every possible defect. Often, genetic screening is used to look for specific genes or proteins that indicate a particular disorder. Also helps with finding diseases like Breast Cancer and …show more content…
It can also lead to some difficult choices. Suppose a person family history who has had quite a few people have cancer and is tested? What should they do? Well they would first probably go for Genetic Screening to test and see if they have it. If a person has a chance of being a carrier of a genetic disorder, How would it affect the rest of their lives? As genetic screening becomes more common, more question like these will need to be answered. Genetic screening is very useful for finding all kinds of diseases that cause your chromosomes to be missing their X’s or Y’s. A Male is XY, a female is a XX. But people sometimes end up with XXY(Klinefelter's Syndrome) click Here to learn more about disorders and how scientists can spot them (paper done by me). There are also tests for about 900 genetic disorders, including cystic fibrosis and Duchenne’s muscular dystrophy (DMD). In DMD, it is quite easy to see differences in DNA tests between people with and