Science advances in a dizzying way, one of the most advanced sciences has been genomics, this discipline has several branches, functional genomics, structural, pharmacogenetics or molecular diagnosis among others. All these conjugate disciplines will allow in the near future (about 15 years) that doctors and specialists know the development that will show the health of a newborn child throughout his life.
Genomics in general will allow an individualized medicine, when a baby comes to the world, it will leave the parlor with a genetic file in which all those important and necessary aspects will be shown that will serve to know its nutrigenomic profile (the most appropriate type of diet that should lead), Direct to the palate we can find an article that refers to the nutrigenomic and how this science is outlined as the most appropriate to know the right diet for each person. They will know which diseases will be subject to it thanks to the genomic vulnerability profile and even their pharmacogenetic and pharmacogenomic profile can be developed, so that they will be able to know the diseases that they may suffer and the most appropriate treatment to follow.
Currently more than 1,400 genes related to different diseases are known, up to 3,500 genes related to some type of cancer and 3,000 related to certain nervous diseases are known, but research continues and these figures are increased day by day allowing little by little that Genomic discipline is more complete and therefore more effective.
According to the specialists, the benefits obtained from the development of the disciplines that we have mentioned before are very important, Know the risks of suffering from a disease in a child, 30 or 40 years before suffering, will allow effective prevention against it through personalized action plans.
Medicine in 15 years will not look anything like the medicine that parents know today and we are glad, since many problems can be solved before they appear.
