0
What else can I help you with?
A man with hemophilia marries a woman without the disease What is the possible offspring?
All Girls will be carriers of Hemophilia. All Boys will be unaffected (they won't have Hemophilia).
What whoud be the result of a normal women having a child with a hemophilia men?
All Girls will be carriers of Hemophilia and all Males will be unaffected (they won't have Hemophilia).
A woman with hemophilia and a man without hemophilia get married. What are the chances that their first child will have hemophilia?
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.
Did Stacy Romanov and her sisters have hemophilia?
Grand Duchess ANASTASIA and her sisters were probably carriers of the hemophilia gene but did not suffer from the effects of hemophilia. Males suffer from hemophilia. In rare cases girls do suffer but that is only when both parents carry the mutated gene
Females who are carrier for hemophilia?
Females who are carriers of hemophilia possess one normal and one mutated allele of the gene responsible for the disorder, typically located on the X chromosome. While they often do not exhibit severe symptoms of hemophilia due to the presence of the normal allele, they can experience mild bleeding problems and have a 50% chance of passing the mutated allele to their offspring. Male children who inherit the mutated allele will be affected by hemophilia, while female children may become carriers themselves. Genetic counseling is recommended for carriers to understand the risks for future generations.
Does a human offspring inherit hemophilia from the mother or father?
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 .
Should parents get tested for hemophilia before having a child?
Yes. Parents can be carriers of MANY different diseases.
If both parents are carriers what will the child be?
When a recessive trait is inherited from both parents, it will be expressed. If the trait is hemophilia, the child will be a hemophiliac.
Is hemophilia a chromosome abnormality?
Hemophilia is not classified as a chromosome abnormality; rather, it is a genetic disorder caused by mutations in specific genes responsible for blood clotting factors. Most commonly, hemophilia A is linked to mutations in the F8 gene, and hemophilia B is associated with the F9 gene. These genes are located on the X chromosome, which is why hemophilia predominantly affects males, while females can be carriers. Thus, while it involves genetic factors, hemophilia itself is not due to a chromosomal abnormality.
What is the Inheritance pattern of hemophilia?
If the father has hemophilia and the mother is a carrier, sons will have a 50% chance of having hemophilia. Daughters will have a 50% chance of having hemophilia and a 50% chance of being a carrier. It is very rare for both parents to have these defective genes.If the father does not have hemophilia and the mother is a carrier, sons will have a 50% chance of having hemophilia. Daughters will have a 50% chance of being carriers.If the father has hemophilia and the mother has normal blood, all sons will be normal and all daughters will be carriers.
What gender are most people with hemophilia?
You would get it from your mother. It is a sex-liked genetic disorder. Females are the carriers, males exhibit the condition.
What is a carrier for hemophilia?
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.
