In recent years, important discoveries have been made in the field of genetics, thanks to more comprehensive knowledge in this field, various diseases, disorders or anomalies can be detected in time, allowing specialists to make more precise decisions based on diagnoses obtained.
In the field of genetics, the possibilities for a clear and concise prevention of cardiac, carcinogenic or sudden death problems are opened, in fact, it is increasingly common for genetic detection techniques to be used. Today we have heard the news that a Spanish company, Ferrer Incode, will start next year to market some genetic biochips capable of identifying the risk of sudden death. It is a DNA biochip capable of detecting up to 1,500 mutations found in 50 different genes that are associated with various cardiac problems such as congenital arrhythmic syndromes or cardiomyopathies. Especially our attention is focused on all those methods that can avoid health problems in babies, these new tools are able to provide us with greater peace of mind, since knowing the risks, specialists can provide the appropriate treatment that will prevent or at least reduce the possibility of suffer a fatal outcome.
There is no doubt that the genetic detection tools will be the most used in the future, managing to significantly reduce the various problems that affect the health of children.
