Color blindness is typically a sex-linked trait that is associated with the X chromosome. Since males have one X and one Y chromosome (XY) and females have two X chromosomes (XX), the inheritance pattern of color blindness is different for boys and girls.
If a woman carries the gene for color blindness on one of her X chromosomes, she can pass that gene to her children. The possible scenarios for the girl and boy are as follows:
- The boy (with one X chromosome from his mother) has a 50% chance of inheriting the X chromosome that carries the color blindness gene. If he inherits that X chromosome, he will be color-blind.
- The girl (with two X chromosomes) could inherit one normal X chromosome and one X chromosome with the color blindness gene. If she inherits one normal X chromosome from her father (who has a normal vision since males inherit only one X), she will be a carrier but not color-blind. She would need to inherit two X chromosomes carrying the color blindness gene (one from each parent) to actually be color-blind, which is less likely.
Therefore, the boy is more likely to be color-blind from birth, because he only needs one affected X chromosome to express the trait.
The correct answer is: the boy is more likely to be color-blind from birth.