Genetic Diseases Affecting Babies And Children

In the world, there are over 6,000 genetic disease disorders affecting babies and children every day. How do we prevent this from occurring in the next generation? The answer is genetic mutations. Genetic mutations are when you alter a certain gene that could cause a disease such as Cystic Fibrosis or Down Syndrome. However, this isn’t always the case. Besides only using the advanced technology, many people are interested in limiting pain and increasing intelligence in tomorrow’s youth. In my opinion, genetic mutations are acceptable in medical situations, however not to increase intelligence or the appearance of a child in the future. For example, it should be acceptable if a child has an immense chance of contracting a disease that has run in the family bloodline for a protracted time. Yet, people also find it adequate to change the looks or mental capacity of a child. This can be known as wasteful and not a prominent approach to using the experienced
First, it could prevent or even eliminate disease genes and prevent them from passing them on to forthcoming generations (Doc. 3). In past research, people were questioned and their responses were recorded. After all the numbers were added up, it showed 83% of the subjects disagreeing to making a baby more intelligent (Doc. 4). However, only 50% disagreed to reducing the risk of serious diseases (Doc. 4). Why are these numbers so drastically different? The answer is easy; it is less accepted to change the appearance or smarts of a kid than to prevent a troubled future. Picture this: a parent with a history of Cystic Fibrosis decide to have a child. This genetically inherited disease that affects the digestive system is possibly deadly or can complicate the life of a case (OI). If the chances are almost already determined for the child to contract the disease, does that make it approved to genetically prevent