Triple X syndrome is also known as triplo-X, trisomy X, XXX syndrome, 47,XXX aneuploidy. It is a form of chromosomal variation characterized by the presence of an extra X chromosome.
Triple-X syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). Approximately 0.10% or 1 per 1,000 newborn girls suffer from triple X syndrome.
The chromosome change that causes triple X syndrome cannot be repaired, so the syndrome itself has no cure but it's quite possible to live normal life with this syndrome.
Most of the research that has been published on Triple X Syndrome focuses on case studies and medical/physiological data on patients with Triple X Syndrome.