Examining The Blood Disorder Of Haemophilia Biology Essay.
Haemophilia is a rare condition that affects the blood's ability to clot. It's usually inherited. Most people who have it are male. Normally, when you cut yourself, substances in your blood known as clotting factors mix with blood cells called platelets to make your blood sticky and form a clot.
Introduction Hemophilia is a bleeding disorder that is hereditary where the blood clotting process takes place in an abnormal way and it is very rare. People affected by hemophilia may bleed for a longer period especially after an accident.
Hemophilia A is the result of the body not making enough factor VIII. Hemophilia A is caused by an inherited X-linked recessive trait, with the defective gene located on the X chromosome. Females have two copies of the X chromosome.
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Haemophilia is a mostly inherited genetic disorder that impairs the body's ability to make blood clots, a process needed to stop bleeding. Those with a mild case of the disease may have symptoms only after an accident or during surgery.
Essay Hemophilia Tim Poisal Biology-2nd period Hemophilia is a genetic blood disease, which is characterized by the inability of blood to clot, or coagulate even from minor injuries. This disease is caused by an insufficiency of certain blood proteins, called factors, that participate in blood clotting and often by sudden gene mutation.
Haemophilia is caused by an inherited change to a gene. It mainly affects males. How the mutation is inherited. The gene change is on the X chromosome. It can be carried by either the mother or father, or both. The chances of a child inheriting the haemophilia changed gene depends on which of their parents has the changed gene.