What is haemophilia ?write it's ex linked in inheritance pattern
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Hemophilia A and hemophilia B are inherited in an X-linked recessive pattern. The genes associated with these conditions are located on the X chromosome, which is one of the two sex chromosomes. In males (who have only one X chromosome), one altered copy of the gene in each cell is sufficient to cause the condition.
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Hemophilia is a rare type of bleeding disorder that occurs when there is a deficiency or absence of a particular protein (clotting factor) needed for blood to clot. As a result, a person with hemophilia will experience longer bleeding after an injury because the clot formed is not strong enough to stop the bleeding.
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