The possibility of a female becoming haemophilic is extremely rare because the mother of such a female has to be at least (i) and father should be (ii).
A. (i) Haemophilic, (ii) Carrier
B. (i) Carrier, (ii) Haemophilic
C. (i) Haemophilic, (ii) Normal
D. (i) Haemophilic, (ii) Haemophilic
Answer
612.3k+ views
Hint: Haemophilia is a rare genetic condition where the individual experiences a distorted blood clotting mechanism. It is also known as The Royal disease because it affected the royal families of England, Germany, and Russia. In this, the males are mostly affected while females may lead a normal life even when they have defective genes on one of their X chromosomes.
Complete answer:
Hence, the correct answer is option (B).
Note: Haemophilia is a rare inherited condition where the individual lacks the blood clotting abilities. The factors responsible for blood clotting are absent in such individuals and thus, this can often lead to serious blood loss in injured situations, severing the consequences further.
Complete answer:
Haemophilia is an inherited recessive sex-linked genetic disorder. In this condition, the person lacks the blood clotting factors. Thus, such individuals show prolonged bleeding even from minor injuries. In females, there are XX chromosomes whereas in males it is XY. So, a female is hemophilic (or said to be affected with haemophilia) if she has both the X chromosome and possesses the defective gene responsible for hemophilia. However, a male is found to be haemophilic if he has the defective gene for haemophilia on his X chromosome, causing the individual to lack factors essential for blood clotting.
A female with the defective gene on only one of the X chromosomes is normal, and said to be only a carrier for this genetic disorder (haemophilia) because the other X chromosome has the gene for normal blood clotting. Therefore, a female is haemophilic only when she has homozygous recessive genes for the trait, that is, her father must be haemophilic contributing for providing one defective paternal X chromosome, and mother must be at least a carrier to provide another X chromosome with a defective gene responsible for hemophilia.
Thus, the correct answer is option B. The availability of another X chromosome in females makes them less prone to Haemophilia. The father must be affected with haemophilia, and the mother should at least be a carrier for the disorder so as to have a haemophilic daughter.
Note: Haemophilia is a rare inherited condition where the individual lacks the blood clotting abilities. The factors responsible for blood clotting are absent in such individuals and thus, this can often lead to serious blood loss in injured situations, severing the consequences further.
Recently Updated Pages
Master Class 12 Business Studies: Engaging Questions & Answers for Success

Master Class 12 Chemistry: Engaging Questions & Answers for Success

Master Class 12 Biology: Engaging Questions & Answers for Success

Class 12 Question and Answer - Your Ultimate Solutions Guide

Master Class 11 English: Engaging Questions & Answers for Success

Master Class 11 Social Science: Engaging Questions & Answers for Success

Trending doubts
Which are the Top 10 Largest Countries of the World?

Draw a labelled sketch of the human eye class 12 physics CBSE

Differentiate between homogeneous and heterogeneous class 12 chemistry CBSE

Differentiate between Pyramid of energy and pyramid class 12 biology CBSE

Why is the cell called the structural and functional class 12 biology CBSE

Draw the diagram of the pyramid of energy Explain In class 12 biology CBSE

