Hemophilia is passed down from mother to son. It is extremely
rare for a woman to have hemophilia. It is necessary, though, for
a woman to be a carrier of the disorder for her son to acquire this
disorder. Females have two X chromosomes whereas males only
have one. When a boy is born, he takes one X chromosome from
his mother and one Y chromosome from his father. Therefore, he
can only get hemophilia through his mother.
Example One:
Mother(Carrier)+Father(Non-Affected)=50% chance of their son
acquiring the disorder and 50% chance of their daughter being a
carrier.
Example Two:
Mother(Non-Affected)+Father(Hemophiliac)=All sons will be
non-affected and all daughters will be carriers.
A carrier for hemophilia is a female who carries the genetic mutation for hemophilia on one of her X chromosomes, but does not exhibit symptoms of the condition herself. Carriers can pass on the gene mutation to their children, resulting in hemophilia in male offspring. Testing can confirm carrier status.
The genotype of Alice of Hesse is Tt and Leopold is tt.
Hemophilia is caused by a deficiency of clotting factor VIII (hemophilia A) or clotting factor IX (hemophilia B).
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.
50 million ppl have hemophilia
All Girls will be carriers of Hemophilia. All Boys will be unaffected (they won't have Hemophilia).
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.
Hemophilia is not contagious by any means, however it can be passed from parent to offspring in the way of genetics.
While the condition affects the males, it is CARRIED by the females, who do not suffer the effects of hemophilia, and can pass the disorder to THEIR female offspring.
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 .
Without any further information, the probability is between 0.0001 and 0.0002
A carrier for hemophilia is a female who carries the genetic mutation for hemophilia on one of her X chromosomes, but does not exhibit symptoms of the condition herself. Carriers can pass on the gene mutation to their children, resulting in hemophilia in male offspring. Testing can confirm carrier status.
The genotype of Alice of Hesse is Tt and Leopold is tt.
Yes, xHxH can represent a female carrier of hemophilia, where "H" denotes the hemophilia allele and "x" denotes the normal allele. In this case, the individual has one normal allele and one allele for hemophilia. However, a female carrier typically does not exhibit symptoms of hemophilia but can pass the allele to her offspring. Males with the genotype "xHy" (where "y" is the male chromosome) would express the condition due to having only one X chromosome.
Hemophilia is one disease in which blood does not clot normally. von Willebrand's Disease
There is no chance that the child will have hemophilia even if the spouse has hemophilia. Any girls the couple has will be carriers if the spouse has hemophilia.
50%