A genetic disease is a disorder that occurs because a gene has a different shape than it should be or there are abnormalities in the chromosomes. Some genetic disorders are inherited and can be passed from generation to generation.
Genetic tests play a big role here. But are we really prepared to accept the results that genetic tests can show us and live knowing them? Currently, thanks to these tests, it is possible to diagnose the diseases or ailments that we may develop in the future or to know what their evolution will be. The results of genetic tests will reveal the diseases we suffer from, but this does not mean that they will necessarily manifest themselves.
In relation to cardiovascular diseases , the highest percentage of heart attacks occur in people who are not subject to preventive measures because they have a low or moderate risk of suffering them. In this case, if the results of genetic tests reveal that we have a predisposition to cardiovascular diseases, the greatest benefit that personal genetic information will bring us will be useful to anticipate and prevent future appearance of health problems like these. We cannot control our DNA, but we can know what we are prone to and thus be able to take better care of ourselves, control what we eat, if we exercise, if we sleep and rest enough or if we have a lot of stress.
Performing genome sequencing tests to find out information about the origin or possibility of developing specific diseases is especially indicated when there is evidence of a family history of inherited diseases such as cardiovascular problems, cancer or neurodegenerative diseases. Detecting them early can save your life.