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.
No actually it is a sex-linked trait.
This combination XXY produces a male child with Klinefelter's Syndrome.
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.
This combination XXY produces a male child with Klinefelter's Syndrome.
This combination XXY produces a male child with Klinefelter's Syndrome.
Yes, individuals with XXY chromosomes (Klinefelter syndrome) can still father children. However, they may have reduced fertility due to lower sperm count and quality. It is advisable for them to consult a healthcare provider for fertility options.
47,XXY. This means that he has 47 chromosomes, including 2 X chromosomes and 1 Y chromosome.
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.
Normal male humans have the sex chromosomes XY. The presence of the Y chromosome determines sex in humans - so a person with XXY will be male.
Yes, individuals with an XXY chromosome combination have a condition known as Klinefelter syndrome. This can affect physical development and may lead to infertility, but gender identity is not solely determined by chromosomes.
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.