Males.
Hemophilia is sex linked. Males inherit from their mother, daughters are carriers if the defective gene is inherited from one of either parent. A female must inherit two copies of the defective allele to have hemophilia .
Anyone can inherit hemophilia. In most cases, it is a man whose mother is a carrier of the disease. It is extremely rare for a woman to have hemophilia but it is not uncommon for one to be a carrier. It is even possible for someone whose family has no record of hemophilia to get it through gene mutations.
There are no hard answers to this, it depends strictly on luck. The statistics are though not very good for their children. Statisically the couple have a chance of having a normal son, a daughter that is a carrier for hemophilia, a daughter with hemophilia and a son with hemophia.
Recessive?? (i.e., you would need to inherit one from each parent to have hemophilia)
Male hemophiliacs inherit it from their mother, because hemophilia is only on the X gene and males only have one and it is from their mother.
recessive trait. This means that males are more likely to express hemophilia because they only have one X chromosome. Females can be carriers of the hemophilia allele if they inherit it on one of their X chromosomes.
The father is the one who can pass the allele for hemophilia to a daughter. Hemophilia is a recessive X-linked disorder, so the daughter would need to inherit the hemophilia allele from her father.
It is a sex-linked recessive trait inherited from the mother.
That will depend on the wording of the will. Their children are more likely to inherit if there are any.
Yes, royal hemophilia, also known as the "Royal disease," is a hereditary bleeding disorder caused by a mutation in the gene responsible for producing a blood clotting protein. It is inherited on the X chromosome. Because males have only one X chromosome, they are more likely to express the hemophilia trait if they inherit the mutated gene.
Males only have one copy of the X chromosome
Yes, there is nothing stopping a person with hemophilia from having children. There are several concerns a person with hemophilia should be aware of though when the time comes to have children. The first, and most obvious would be the chance for blood loss and uncontrolled bleeding during the birthing process if the mother is the one with hemophilia. While this is something to be aware of, it is also something that can be easily prepared for and overcome. In this situation, the chances of having sons and daughter who inherit the traits for hemophilia is very likely. If the mother had the genes for hemophilia on both X chromosomes, all of her children will inherit the trait (daughters may or may not be symptomatic while all sons will be). If the mother only had the trait on one of her two X chromosomes, then there is a 50% each child born would receive the trait. Since the trait for hemophilia is located on the X chromosome, and males have only one of these X chromosomes, all daughters of a male with hemophilia will receive the genes for hemophilia from him while any sons he has will not receive the gene.