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Turner Syndrome is a genetic disorder that affects approximately 1 in 2,500 female live births. It is characterized by the complete or partial absence of one X chromosome, resulting in only one functioning X chromosome in the body's cells. This chromosomal aberration can lead to a range of physical and developmental symptoms, such as short stature, ovarian dysfunction, heart defects, and learning disabilities. In the context of Science, Genetics, and Recombination, Turner Syndrome provides an important example of how chromosomal abnormalities can impact human health and development. From a genetics perspective, it illustrates the importance of having two functioning copies of each chromosome for normal growth and development. Additionally, recombination events during meiosis can result in nondisjunction, leading to aneuploidy and conditions like Turner Syndrome. Furthermore, studying Turner Syndrome can provide insights into the genetic mechanisms underlying sex determination and differentiation, as well as the role of X chromosome dosage in various biological processes. Overall, it is a critical area of study that contributes to our understanding of genetics, recombination, and chromosomal aberrations.