Nondisjunction will occur . Yep
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.
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.
An embryo, male or female, usually has two sex chromosomes, one from mom, one from dad. In a male's case, they would be XY. Rarely, nondisjunction occurs, and a child winds up XXX, XXY, XYY, or X. XXX and X become female, and XXY and XYY become male. So, it is theoretically possible for a male embryo to have three sex chromosomes.
No actually it is a sex-linked trait.
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.
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.
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.
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.
An embryo, male or female, usually has two sex chromosomes, one from mom, one from dad. In a male's case, they would be XY. Rarely, nondisjunction occurs, and a child winds up XXX, XXY, XYY, or X. XXX and X become female, and XXY and XYY become male. So, it is theoretically possible for a male embryo to have three sex chromosomes.
No actually it is a sex-linked trait.
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.
XXY. Klinefelter is caused when the X chromosomes of the mother fail to split, or an XY sperm reaches an X egg, resulting in a mostly male child.
1 pair of sex chromosomes Female pair is XX Male pair is XY
It is the father's contribution that determines the sex of the offspring. Of the XX and XY pairs that determine sex, the mother always contributes an X. If the father contributes an X as well, the offspring is female. If the father contributes a Y, the offspring is male.
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.
Humans have 46 chromosomes, with 22 pairs of autosomes and 1 pair of sex chromosomes. Males have XY sex chromosomes while females have XX sex chromosomes. However, genetic disorders do occur whereby some males have XYY or XXY chromosomes, making the total number of chromosomes to be 47. Females have their own share of genetic disorders: Turner's Syndrome (single X chromosome) or Trisomy X (XXX). In normal cases the short answer would be: XY for males, XX for females.
Two. Either XX for female and XY for male. This is standard issue and not always the number. XXY Kleinfeter's syndrome in males X Turner's syndrome in females As examples of chromosome disjunction that happens in humans. Not always fatal and not very deleterious, but noticeable in phenotype expression.