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Describe how the karyotype of an XXY human would differ from that of an XO human?
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.
What is a baby's gender if he or she has XXY sex chromosomes?
A baby with XXY sex chromosomes typically has Klinefelter syndrome, which is associated with male development. However, individuals with XXY chromosomes can have a range of physical and developmental differences. It's important to remember that gender identity is separate from biological sex.
What Traits controlled by genes located on sex chromosomes are what kind of traits?
The Y chromosome controls sex because the SRY region( sex determining region ) is on this chromosome. XX is female as default. This is subject to some variation, as the SRY region sometimes ends up on an X chromosome and you have various chromosome distributions too. X, XXY, and the like. Other than that, there are too many traits that are under control of these chromosomes to list here.
What causes disorders such as klinefelter syndrome and turner syndrome?
Klinefelter syndrome is a chromosomal condition that only affects males and is characterized by a male having an additional X chromosome (XXY) in cells. This chromosome abnormality occurs when there is an error in cell division, resulting in an extra copy of the X chromosome.
What genetic disorder has 44 autosomes and 3 or more sex chromosomes?
The genetic disorder you are referring to is Klinefelter syndrome. Individuals with Klinefelter syndrome have 44 autosomes and at least one extra sex chromosome, usually XXY. This condition can lead to various physical and developmental differences in affected individuals.
What would a male with the sex chromosomes xxy have?
A male with the sex chromosomes XXY would have Klinefelter syndrome, a genetic condition that can result in low testosterone, reduced fertility, and other possible physical and developmental traits.
Is there a cure for xxy syndrome?
As on today, there is no cure for xxy syndrome.
Describe how the karyotype of an XXY human would differ from that of an XO human?
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.
What is the duration of XXY film?
The duration of XXY - film - is 1.45 hours.
Which one of the following genotypes causes klinefelter syndrome xy xx xxy or xyy?
Yes, Klinefelter's syndrome is due to the XXY genotype.
What designates a normal human female 1. XXY 2. XY 3. XX 4. XYY 5. XO?
xx designates a normal human female.
What actors and actresses appeared in Xxy - 1995?
The cast of Xxy - 1995 includes: Caroline Berg
What kind of mutation occurred to produce a person with the genotype XXY?
The genotype XXY is associated with Klinefelter syndrome, which arises from a nondisjunction event during meiosis. This mutation results in the failure of homologous chromosomes or sister chromatids to separate properly, leading to an extra X chromosome in males. Consequently, individuals with XXY typically exhibit male characteristics but may experience various physical and developmental differences.
What chromosomal abnormality causes Klinefelter syndrome?
46,XXY or XXY for males; see the link below.
What is a baby's gender if he or she has XXY sex chromosomes?
A baby with XXY sex chromosomes typically has Klinefelter syndrome, which is associated with male development. However, individuals with XXY chromosomes can have a range of physical and developmental differences. It's important to remember that gender identity is separate from biological sex.
What are the genetics behind Klinefelter's syndrome?
Klinefelter Syndrome is not caused by genes but is rather caused by chromosomal nondisjunction, or an odd number of chromosomes. Klinefelter Syndrome is particularly the presence of more than one X chromosome in a male's karyotype in addition to one Y chromosome (normal males have one X and one Y). Typically, a Klinefelter patient will feature the XXY karyotype, although the presence of additional X chromosomes has been reported. The adverse phenotypes associated with Klinefelter Syndrome are due to complications arising from gene dosage, or the amount of gene expression, not due to the presence of a certain gene or mutation.
What genotypes cause Klinefelter's syndrome?
The only genotype to cause Klinefelter's syndrome is XXY.
