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.
Hemophilia does not follow classic Mendelian inheritance patterns because it is an X-linked recessive disorder. This means that the gene responsible for hemophilia is located on the X chromosome, and males, having only one X chromosome, are more likely to express the condition if they inherit the affected allele. In contrast, females have two X chromosomes, so they would need to inherit two copies of the mutated gene to exhibit the disorder, making hemophilia less common in females. This results in a characteristic inheritance pattern that diverges from Mendelian ratios typically seen in autosomal traits.
Hemophilia is typically an X-linked recessive condition. If a mother has hemophilia, she carries two copies of the hemophilia allele on her X chromosomes (since females have two X chromosomes). Therefore, any male offspring will inherit one of her X chromosomes, which will carry the hemophilia allele, leading to him being affected by the condition. The male will inherit his Y chromosome from his father, which does not carry the hemophilia gene.
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.
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.
That will depend on the wording of the will. Their children are more likely to inherit if there are any.