The 4 Most Common Genetic Conditions in the US
Genetics is one of the most complex issues that exist, with various cases that have impacted the world by the number of disorders or conditions that can develop through DNA as an inheritance of a family member. Here we bring you some of the most common genetic conditions in the US:
According to studies carried out, there is half the probability that someone can transmit this same disease to their child in case one of their parents has it. And the most curious thing about this disease is that it’s usually detected after 30 years.
This is an anomaly in the chromosomes of pair 21, causing mental and developmental delay. Normally this disease is detected once the child is born, but some cases have been detected before being born with prenatal tests.
Duchenne Muscular Dystrophy
This disease is characterized by progressive muscle weakness in people, usually detected from children. In addition, it’s more common in children who have a certain delay or a heart or respiratory problem.
Cystic fibrosis is a genetic and hereditary disorder commonly when both parents are carriers, which affects the lungs and the digestive system. The cure hasn’t yet been found, so all sufferers must undergo treatments to try to control this difficult disease.
Genetics is something unpredictable, something that nobody can control. They’re biological and parental issues that you should simply assume, understand and start to treat seriously and medically.