A man with a genetic disease marries a woman who does not carry the disease. It is not possible for their son to carry the disease. The disease must be?

The disease must be an X-linked disease (both dominant and recessive are possible), or a recessive trait.

The son will inherit one of his mom's X chromosomes and his dad's Y chromosome. If it is impossible for the son to get it, it certainly is not located on the Y chromosome, which he will get from his dad.

It could be on his dad's X chromosome, either dominant or recessive, and he would have a 0% chance of getting it, since he will not get his dad's X chromosome.

It could also just be a recessive, non sex-linked trait, in which case he could not possibly get it because his mom is not a carrier.

JoiePatel JoiePatel · Answer 2 · 2019-03-14T12:33:28+01:00

Answer:

The correct answer would be X-linked.

X-linked diseases are those the genes of which are present on the X-chromosome.

In humans, the males are heterozygous for sex chromosomes, that is, they are XY whereas the females are homozygous, that is, they are XX.

The male inherited only the Y chromosome from the father and X chromosome from the mother whereas the daughter receives one X chromosome from the father and another X from the mother.

Thus, if the disease is X-linked (whether dominant or recessive) and mother is normal then the disease can not pass from the diceased father to his son.