
Why is haemophilia more common in males?
Answer
498k+ views
Hint: Hemophilia is a bleeding disorder caused by a genetic defect due to which blood doesn't clot correctly. Due to hemophilia patients may experience uncontrolled bleeding after an injury or a surgery. This happens because of the deficiency of clotting factors in the blood. Excessive bleeding (both exterior and internal) happens after any accident or damage when blood cannot clot correctly.
Complete answer:
This question can be solved by putting the logic of X linked inheritance, which is defined as the inheritance of genes present on only X chromosome.
Humans have \[46\] chromosomes; one half of this set is derived from the mother while the other half is derived from the father. Males have a single “X” and a single “Y” chromosome, whereas females have two “X” chromosomes (XX) (XY). Mutations on the X-chromosome are connected to X-linked diseases. Because females have an extra X chromosome that functions as a "back-up," these diseases afflict men more frequently than females.
Because males only have one X chromosome, haemophilia is caused by a mutation in the factor VIII or IX gene. “Carriers” are females who have a mutation on one X chromosome.
Thus, due to the presence of a single copy of X chromosome in males makes them much more susceptible to inherit the disorder.
Note:
Hemophilia A and B have an X-linked recessive inheritance pattern. The X chromosome, which is one of the two sex chromosomes, contains the genes related with these diseases. Hemophilia A (also known as classic haemophilia or factor VIII deficiency) and haemophilia B are the two most common forms (also known as Christmas disease or factor IX deficiency).
Complete answer:
This question can be solved by putting the logic of X linked inheritance, which is defined as the inheritance of genes present on only X chromosome.
Humans have \[46\] chromosomes; one half of this set is derived from the mother while the other half is derived from the father. Males have a single “X” and a single “Y” chromosome, whereas females have two “X” chromosomes (XX) (XY). Mutations on the X-chromosome are connected to X-linked diseases. Because females have an extra X chromosome that functions as a "back-up," these diseases afflict men more frequently than females.
Because males only have one X chromosome, haemophilia is caused by a mutation in the factor VIII or IX gene. “Carriers” are females who have a mutation on one X chromosome.
Thus, due to the presence of a single copy of X chromosome in males makes them much more susceptible to inherit the disorder.
Note:
Hemophilia A and B have an X-linked recessive inheritance pattern. The X chromosome, which is one of the two sex chromosomes, contains the genes related with these diseases. Hemophilia A (also known as classic haemophilia or factor VIII deficiency) and haemophilia B are the two most common forms (also known as Christmas disease or factor IX deficiency).
Recently Updated Pages
Which cell organelles are present in white blood C class 11 biology CBSE

What is the molecular geometry of BrF4 A square planar class 11 chemistry CBSE

How can you explain that CCl4 has no dipole moment class 11 chemistry CBSE

Which will undergo SN2 reaction fastest among the following class 11 chemistry CBSE

The values of mass m for which the 100 kg block does class 11 physics CBSE

Why are voluntary muscles called striated muscles class 11 biology CBSE

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

What are the major means of transport Explain each class 12 social science CBSE

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

Draw the diagram showing the germination of pollen class 12 biology CBSE

Differentiate between insitu conservation and exsitu class 12 biology CBSE

The computer jargonwwww stands for Aworld wide web class 12 physics CBSE

