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The human is classified a male. Physical traits include male sex organs, but small testes. They are sterile. Can have some breast enlargement and other female characteristics which are common.
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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 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 is the sex chromosome makeup for a human male?
XY. XX is the female. Of course, anomalies occur: XXY, XXX, etc., in instances where the earliest cell division either fails to separate fully or when one of the partners carry a similar anomaly and still remain reproductive and viable.
Why is monosomy worse than trisomy?
Monosomy occurs when one chromosome is absent from the normal diploid number. This is referred to as aneuploidy which is the loss or gain of a chromosome during meiosis.An example of monosomy is Turner Syndrome. One of the sex chromosomes is missing. In an unaffected female there are 2 'X' chromosomes. But in Turner Syndrome there is one sex chromosome missing.Trisomy occurs when there is three copies of a chromosome instead of the normal diploid number. This is also referred to as aneuploidy because there was an extra chromosome added hence, an abnormal amount of chromosomes.An example of trisomy is in Trisomy 21(Downs Syndrome) in which chromosome 21 has an extra chromosome.
What is a baby's gender if he or she has XXY sex chromosomes?
Male - in humans the sex is determined by the presence of a Y chromosome. In other animals sex can be determined by the ratio of sex chromosomes, or the total number of chromosomes.
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 chromosomal abnormality causes Klinefelter syndrome?
46,XXY or XXY for males; see the link below.
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.
The product of 72 and a number?
72=XxY
What is the karyotype of klienfeter syndrome?
47, XXY
It is possible to assert that resulted in nondisjunction in?
xxy; oogenesis
