Home
Class 12
BIOLOGY
A normal woman, whose father had haemoph...

A normal woman, whose father had haemophilia married normal man . What is the chance of occurrence of haemophilia in their children ?

A

25% children will be haemophilic

B

50% children will be haemophilic

C

75% chilidren will be haemophilic

D

None haemophilic but 75% will be

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem of determining the chance of occurrence of hemophilia in the children of a normal woman whose father had hemophilia and a normal man, we can follow these steps: ### Step-by-Step Solution: 1. **Understand the Genetics of Hemophilia**: - Hemophilia is a sex-linked recessive disorder caused by a defective gene on the X chromosome. Males (XY) are more likely to be affected because they have only one X chromosome, while females (XX) can be carriers if they have one affected X chromosome. **Hint**: Recall that males are affected more than females due to their single X chromosome. 2. **Determine the Genetic Makeup of the Woman**: - The woman’s father had hemophilia, which means he had the defective X chromosome (Xh). Since she is normal, she must have inherited one normal X chromosome (X) from her mother and the affected X chromosome (Xh) from her father. Therefore, her genotype is XhX (carrier). **Hint**: Remember that daughters inherit one X chromosome from each parent. 3. **Determine the Genetic Makeup of the Man**: - The man is normal, which means he has a normal X chromosome and a Y chromosome. His genotype is XY. **Hint**: Males inherit their X chromosome from their mothers and their Y chromosome from their fathers. 4. **Set Up a Punnett Square**: - To find the possible genotypes of their children, set up a Punnett square with the woman’s alleles (Xh and X) on one side and the man’s alleles (X and Y) on the other side. ``` X Y ---------------- Xh | XhX | XhY | ---------------- X | XX | XY | ---------------- ``` 5. **Analyze the Results**: - From the Punnett square, we can see the possible genotypes of the children: - XhX: Female carrier (normal) - XX: Normal female - XhY: Male with hemophilia - XY: Normal male - This results in: - 1 carrier female (XhX) - 1 normal female (XX) - 1 affected male (XhY) - 1 normal male (XY) 6. **Calculate the Probability**: - Out of the four combinations: - 1 child (XhY) will have hemophilia. - Therefore, the chance of having a child with hemophilia is 1 out of 4, or 25%. **Hint**: Count the total possible outcomes and how many of those outcomes result in hemophilia. ### Final Answer: The chance of occurrence of hemophilia in their children is **25%**.
Promotional Banner

Similar Questions

Explore conceptually related problems

A normal women whose father had haemophilia married a normal man. What is the change of occurrence of disease in the progeny?

A haemophiliac woman marries a normal man then :

A normal woman whose fateher was colour blind marries a normal man .the progencyt would be

A normal woman whose father was colour blind is married to a normal man. The sons would be

A normal woman, whose father was colour blind is married to a normal man. The sons would be

A normal woman whose father was haemophilic (X^(h)Y) marries a normal man (XY). The offspring shall be

A normal woman whose father was colour blind, is married to a normal man. The sons would be