answersLogoWhite

0


Best Answer

50%

User Avatar

Kyla Klocko

Lvl 13
2y ago
This answer is:
User Avatar
More answers
User Avatar

Wiki User

14y ago

If the female is not a carrier of hemophilia herself then any male born to the couple would be free of the disease, but all the females would end up being carriers. The reason for this is sex linked. The gene for hemophilia happens on the X chromosome so males who get their X chromosome from their mothers would be free, but since a female gets an X from both parents would be a carier.

This answer is:
User Avatar

User Avatar

Wiki User

13y ago

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.

This answer is:
User Avatar

User Avatar

Wiki User

15y ago

All of her children will carry the gene responsible for hemphilia; however the males may be the only to express its effects. It is due to an abnormal X chromosome and the normal male will give a normal X to cover the recessive or abnormal X in the female children-thus no expression of hemophilia.

This answer is:
User Avatar

User Avatar

Wiki User

14y ago

Women do not get haemophilia ( or factor 8 deficiency ) but they do carry it. Â?They have no symptoms themselves, but pass it on to their male children, who would have symptoms.


I advise you to ask your doctor to test your blood and your husband's blood. Â?Once those results are available, he will be in a position to offer 'genetic counselling'. Â?

This answer is:
User Avatar

User Avatar

Wiki User

12y ago

1/4 or 25%

This answer is:
User Avatar

Add your answer:

Earn +20 pts
Q: A woman with hemophilia and a man without hemophilia are expecting a baby boy. What are the chances that their son will also have hemophilia?
Write your answer...
Submit
Still have questions?
magnify glass
imp
Related questions

What Woman with hemophilia and a man without hemophilia are expecting a baby boy. What are the chances that their son will also have hemophilia?

50%


If a woman with hemophilia and a man without hemophilia are expecting a baby boy. What are the chances that their son will also have hernophilla?

50%


What A woman with hemophilia and a men without hemophilia get married . what are the chances that their first child will have hemophilia?

50%


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.


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).


A woman is a carrier for hemophilia what is the chances for sons with hemophilia if the father does not have hemophilia?

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.


A woman with hemophilia and a man without hemophilia are expecting a baby boy what are the chances that their son will also have hemophilia?

If the female has what is classically defined as female hemophilia (carries the mutation on both of her X chromosomes), then all sons she would have would also have hemophilia. All of the woman's daughters would also inherit the gene, however since they would also be getting a normal X chromosome from their father, they would not, themselves, have hemophilia under the classical definition. Today, it is understood that even carrying the trait on a single X chromosome can reduce a female's factor levels and give cause for doctors to diagnose her with hemophilia. Thus if you are simply looking at genetics (which you probably are) then the answer is all of her sons would have it and all of her daughters would be carriers. Therefore, since there is a 50-50 chance the first child bore would be a male, and a 50-50 chance it would be a female, the chance that their first child born would have hemophilia is 50%.


What are a woman chance of being a carrier for hemophilia if she phenotypically a normal woman and has phenotypically normal parents but has a hemophiliac brother?

She has 1/2 chance. We can figure out exactly what her parents' genotypes were. Her brother has a Hemophilia allele that he got from his mom. So their mom has at least 1 Hemophilia allele. If she had 2 then she would have Hemophilia. The father cannot have a Hemophilia allele because it would have been expressed. So her chances are 1/2 because her mother has 1 Hemophiliac and 1 normal allele.


What is true of a woman with the genotype?

She is a carrier of hemophilia but does not have the condition


If you know a woman has hemophilia what can you infer about her parents genetype?

Her father has to have hemophilia as well, and the mother is a carrier or also has hemophilia. So if we pretend that the hemophilia gene is "x", you need to have "xx" to have hemophilia. The father must have the genotype "Yx" and the mother has the have "Xx" or "xx".


True or false woman can be born with hemophilia?

It is possible but extremely rare.


What gene does hemophilia affect?

The gene that causes hemophilia is located on the X chromosome. A woman who gives birth to a child with hemophilia often has other male relatives who have hemophilia. Sometimes, a baby will be born with hemophilia when there is no known family history. This means the gene can be"hidden"( or passed down through several generations of female carriers without affecting any male members of the family) or the change in the X chromosome is new (a spontaneous mutation).