The karyotype of a person with Down syndrome differs from a normal karyotype because it contains a three chromosomes in the 21st slot, where there should only be a pair of two. That is why this is called Trisomy 21.
Klinefelter's syndrome is not considered to be a variation of normal, so by definition it is abnormal.
The parents have normal genotypes, because Klinefelter's syndrome is not inherited.
No. People with Klinefelter's syndrome have a normal Y chromosome and 2 normal X chromosomes.
Individuals with Klinefelter's syndrome have an extra X chromosome, resulting in a total of 47 chromosomes, with the usual sex chromosomes XX for females and XY for males being XXY in individuals with Klinefelter's syndrome.
Klinefelter = XXY Turner's = X Klinefelter syndrome is the extra X and can lead to somewhat of a female secondary sexual characteristic in men. Turner's is the single X some women receive and can cause short stature and lack of secondary sexual characteristics.
The majority of people with schizophrenia have normal karyotypes. If the karyotype is abnormal, it will be a coincidence and not the cause of the schizophrenia. For example, you can have Turner syndrome (1 X chromosome) and schizophrenia at the same time, but the Turner syndrome wouldn't have caused the schizophrenia.
Klinefelter's syndrome is caused by nondisjunction, which occurs during meiosis when chromosomes fail to separate properly. This results in an individual having an extra X chromosome, leading to the genetic makeup of 47,XXY instead of the typical 46,XY. The presence of the extra X chromosome disrupts normal male development and can result in various physical and developmental characteristics associated with the syndrome. Ultimately, nondisjunction results in the abnormal chromosome number that defines Klinefelter's syndrome.
Most of the Klinefelter Syndrome affected persons can lead a life which could be considered as normal. However, they might have certain problems related to sexual organs, (among others), and some, - but not all -, could be infertile. The reason for this is their extra chromosome. Females have XX chromosomes, Males have XY chromosomes, and Klinefelter syndrome affected males have XXY chromosomes. They often are prescribed testosterone therapy. More info could be found on related links.
Normal humans have 46 chromosomes (23 from each parent). Males with Klinefelter's Syndrome have 47 chromosomes and therefore have acquired an extra chromosome from a parent (hopefully a more knowledgeable contributor will say if it is from the male or female parent). A lot of studies have been done on the male calico cat. Back in the 1980's if one found a male calico cat that was NOT sterile, the cat was worth about 30K... a lot of money for that time period. I am not sure if similar hunts are currently underway.
The karyotype of an XO human would be deficient one X chromosome, compared to that of a normal female, and it would result in a female. Normal human females only use one X chromosome, whereby one is inactivated, which is why an XO human is viable. An XXY human would have one extra X chromosome as compared to that of a normal male, and it would result in a male. Again, an X chromosome is inactivated, which is why an XXY human is viable. XO is referred to as Turner Syndrome. XXY is referred to as Klinefelter Syndrome.
The 23rd pair of chromosomes in humans is the sex chromosomes, with females having two X chromosomes (XX) and males having one X and one Y chromosome (XY). Any abnormality in this pair can lead to conditions such as Turner syndrome (XO), Klinefelter syndrome (XXY), or Triple X syndrome (XXX).
Klinefelter's syndrome is not a mutation; rather, it is a chromosomal condition caused by the presence of an extra X chromosome in males, typically resulting in a 47,XXY karyotype. This additional chromosome disrupts normal development, leading to various physical and developmental characteristics. It occurs during the formation of reproductive cells or in early fetal development, rather than being a mutation in a specific gene.