Turner syndrome (TS), also known as Ullrich-Turner syndrome, is a chromosomal genetic disorder that affects approximately 1 female infant born living in 2,000. This disorder is caused by the absence of genetic material from one of the sex chromosomes during fetal development; other developmental problems occur after birth. The sex chromosomes are: X and Y, which are responsible for the development of male (XY) or female (XX). A male fetus inherits the X chromosome from his mother and the Y chromosome from his father. While female fetuses inherit one X chromosome from each parent. If a woman has Turner syndrome, one copy of the X chromosome is partially missing, altered, or completely missing. The following genetic alterations of Turner syndrome: Monosomy, the The result is that every cell in the fetal body consists only of X chromosomes. Mosaicism can occur during cell division during the early stages of fetal development. When this happens, the cells of the fetus may have two cells...