Fragile X syndrome is known to be a genetic kind of disorder. It happens when there are changes in a genetic history that are known as fragile X mental retardation one, or it is the first thing that you may determine. This gene creates a protein that is known as the fragile X mental retardation protein. It is one of the necessary factors for a normal brain. A person who has syndrome doesn’t have this kind of protein. He/she may have this syndrome because of not having an FMRP. Some few people have fragile X syndrome that is experiencing changes in their gene, but they also have a protein. This syndrome may affect male and female children. Most of the mild symptoms happen in females rather than male.