Yes - this is known as Turner's Syndrome.
Valanga sp. sex is determined by using the XO system. This system use only one type of sex chromosome, the X. Females are XX while males have only one sex chromosome (XO). Sex of the offspring is determined by whether the sperm cell contain and X chromosome or no sex chromosome.
This particular karyotype has 45 chromosomes (instead of the usual 46). "XO" tells us that the karyotype is missing a sex chromosome: the individual has an X, but no homologous sex chromosome (X or Y) to complete the diploid pair.
The term is monosomy, in which one chromosome of a pair is missing. Turner's Syndrome is an example of monosomy, in which there is only one sex chromosome, which is the X chromosome. Humans with Turner's Syndrome are female, but sterile. The genotype of the sex chromosomes in Turner's Syndrome is XO, in which O represents a missing chromosome.
A person with an X and Y chromosome typically identifies as male. The presence of the Y chromosome determines male sex development, leading to the development of male characteristics during puberty.
An XO genotype refers to a genetic condition where an individual has a single X chromosome instead of the typical two sex chromosomes (XX). This condition is known as Turner syndrome and can result in a range of physical and developmental differences.
That isn't physically possible. All XO individuals are females with Turner's syndrome. Individuals with only a Y chromosome do not survive.
Females
Girls with Turner's syndrome
Valanga sp. sex is determined by using the XO system. This system use only one type of sex chromosome, the X. Females are XX while males have only one sex chromosome (XO). Sex of the offspring is determined by whether the sperm cell contain and X chromosome or no sex chromosome.
Nondisjunction -Trisomy 21(Down Syndrome) means there are 3 chromosomes on the 21st pair of chromosomes. -Kleinfelters (XXY) means there is an extra chromosome on the 23rd pair(where the sex chromosomes lie). -Turner Syndrome(XO) On the 23rd pair, there is no Y or second X chromosome. The female can survive with this.
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 XO condition is known as Turner's Syndrome.
The genotype XO results from the absence of a second sex chromosome in an individual. This condition is known as Turner syndrome and is characterized by a single X chromosome in females instead of the usual two. It can lead to various developmental and physical abnormalities.
This particular karyotype has 45 chromosomes (instead of the usual 46). "XO" tells us that the karyotype is missing a sex chromosome: the individual has an X, but no homologous sex chromosome (X or Y) to complete the diploid pair.
Turner syndrome is characterized by an XO chromosome abnormality, where individuals have only one X chromosome instead of the usual two. This condition can lead to various physical and developmental abnormalities, such as short stature, heart defects, and infertility. Treatment may involve hormone therapy and fertility treatment.
The term is monosomy, in which one chromosome of a pair is missing. Turner's Syndrome is an example of monosomy, in which there is only one sex chromosome, which is the X chromosome. Humans with Turner's Syndrome are female, but sterile. The genotype of the sex chromosomes in Turner's Syndrome is XO, in which O represents a missing chromosome.
Y chromosome sperm can survive in the female body for up to 3-5 days before fertilization occurs.