The Klinefelter's Syndrome

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Chromosomes, or strings of genes carrying genetic information, are vital to the existence of living things. A specimen cannot have more or less than how many that particular species needs. In humans, this number is 23. The 23rd pair of chromosomes, referred to as Group X, contain the sex cells that decide the gender of the organism. If a Y chromosome is present, the organism is male, and if not, it is a female. If the chromosomes fail to separate correctly during meiosis (type of cell division that results in sex cells), the chromosomes are not distributed evenly, and is called nondisjunction. This can lead to disorders, such as the Klinefelter’s Syndrome, which is caused by nondisjunction, has symptoms and treatment, is relatively widespread, causes risk for cancer and other illnesses, and is being worked on currently. …show more content…
Dr. Harry Klinefelter was the first to describe the attributes of the genetic disorder, alongside co-workers. Later in the 1950s, it was recognized that KS is caused by having an extra X chromosome, which gives it the name “XXY Trisomy”. In rarer and more extreme cases, a cell may have more than one extra X chromosome. KS is a completely random error, and the parents cannot do anything to risk it, except in older women. It is not inherited, and many recipients of KS live their lives without ever realizing they have

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