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in Biology by (64.2k points)

If these is a history of haemophilia in the family, the chances of male members becoming haemophilic are more than that of the female.

(a) Why is it so ? 

(b) Write the symptoms of the disease. 

1 Answer

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(a) Defective gene is on X chromosome, in case the carrier female (mother) passes Xh to the son he suffers, if she passes Xh to the daughter, she has the other X (from father) to make it heterozygous so the daughters escape as carriers.

(b) The blood does not clot in the affected person after an injury or a small cut.

Detailed Answer :

(a) Haemophilia is a sex linked recessive trait. The gene for this trait is located an X chromosome. There are greater chances of males getting haemophilic because the males have only one X chromosome and haemophilic gene located on this chromosome (XhY) expresses it  self. Human males are hemizygous. Therefore XhY would by haemophilic where XhX would not be haemophilic she will be a carrier. It carrier mother XhX passes Xh to son, he would be haemophilic but if she passes it. to daughter, and she has the other normal X from father, she escapes as carrier.

(b) In haemophilic persons, the blood does not clot after injury due to the absence of blood clotting factor.

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