How can science help people with a specific type of genetic mutation? Firstly, Fragile X Syndrome is a genetic mutation that happens 1 in 4000 males and 1 in 6000 females. Even though it might seem rare, it is still a hard mutation to live with.
Because of this, scientists try to find ways to make the people who are affected have easier and comfortable lives. Next, Fragile X Syndrome is a genetic mutation with specific symptoms, a gene mutation caused by insertion, and it has no treatments. Fragile X Syndrome has many different symptoms. When it comes to learning people with this syndrome have trouble with it. They can have intellectual or developmental disabilities, and they can have hyperactive disorders.
As can be seen, their physical symptoms are having a huge head and ears, flexible joints, flat feet, and a large forehead. Children with Fragile X Syndrome can also be scared in a new and different situation, have attention disorders, and not be able to keep eye contact. They may not talk until later in life, have trouble with stuttering, or have difficulty speaking in full sentences. They can also have sensory issues like sensitivity to light. Doctors can figure out which child has Fragile X Syndrome if they find these symptoms.
Fragile X Syndrome is a genetic mutation that is caused by a insertion. The FMR1 gene on the X chromosome lengthens or expands, and the production of protein is stopped. This protein is responsible for brain development and other functions. A carrier is a person who has a gene that has 50 to 200 repeats. It is called a Fragile X premutation. The carriers can pass on the gene mutation to their children. Male carriers who have daughters pass it onto the daughters, but not to the sons.
Females who are carriers can pass it down to both genders. There are no treatments for Fragile X Syndrome. There are ways that the people affected by the syndrome can have a normalized life. There are special education systems designed for them so that they can learn and develop. As the children grow, they need new medications because new symptoms and difficulties appear.
They can change their way of life so that their life becomes stress-free. Even though they have a genetic mutation with no cure, they can still live life to the fullest. In conclusion, people with Fragile X can have a normal life through special education and help from medical people. Their symptoms specifically show if they have the mutation. The mutation has a complicated process behind it. They can still learn many things, even though it may take longer to learn them. Fragile X victims overcome barriers through different organizations. Overall, People with Fragile X Syndrome have different symptoms, a mutation that is passed down from their parents, and they have medical treatments that make their life easier.