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Haemophilia lowers blood plasma clotting factor levels of the coagulation factors needed for a normal clotting process. Thus when a blood vessel is injured, a temporary scab does form, but the missing coagulation factors prevent fibrin formation, which is necessary to maintain the blood clot. Thus a haemophiliac does not bleed more intensely than a normal person, but can bleed for a much longer amount of time. In severe haemophiliacs even a minor injury could result in blood loss lasting days, weeks, or not ever healing completely. In areas such as the brain or inside joints, this can be fatal or permanently debilitating.

In short, it makes your wounds harder to heal/takes longer for them to heal.
Hemophilia is found in the blood. It is a disease that causes the blood to not clot properly.

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9y ago

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Related Questions

What protein does hemophilia affect?

Hemophilia primarily affects clotting factors in the blood, specifically factor VIII in hemophilia A and factor IX in hemophilia B. These proteins are essential for normal blood coagulation, and their deficiency leads to prolonged bleeding and difficulty in forming clots. As a result, individuals with hemophilia experience increased bleeding risks from injuries, surgeries, or spontaneous bleeding episodes.


How does hemophilia affect society?

It's important for society to know how scary hemophilia can be. Hemophilia is a blood clotting disorder in which it is hard to clot once bleeding has occurred. People that have hemophilia (mostly males) often lose a lot of blood and need donor blood. People in society need to know before they donate blood that their blood is clean (free of AIDS especially). People that have hemophilia are limited to certain activities and need to be extremely careful every minute of every single day.


What is impaired blood clotting?

it is a blood clot which is impaired.


What is a disease in which the blood does not clot normally?

Hemophilia is one disease in which blood does not clot normally. von Willebrand's Disease


What is the effects of Hemophilia?

Hemophilia is when your blood clots slowly or not at all.


How does a healthy gene differ from a gene that causes hemophilia?

A healthy gene does not have mutations that disrupt normal blood clotting factors. A gene that causes hemophilia has mutations that affect the production or function of blood clotting factors, leading to difficulty in blood clotting and increased risk of bleeding.


What inherited disorders makes the blood slow to coagulate?

Hemophilia


What is desire of blood?

Hemophilia


Is Hemophilia mutated allele that produces a defective form of the protein hemoglobin?

False; Hemophilia is caused by a mutated allele that produces a defective form of the protein fibrin.Sickle Cell Disease is caused by a defective form of hemoglobin.


Who studied hemophilia?

Hemophilia is a hereditary blood disease; it is studied by geneticists and hematologists.


What is the disease that prevents blood from clotting?

blood do not clot it is due to disease that disease called haemophiliafromshrey batham ,class 1oU.D.C.A


What is the condition in which blood doesn't clot?

The condition in which blood doesn't clot effectively is known as hemophilia. It is a genetic disorder that results in a deficiency of certain clotting factors, leading to prolonged bleeding after injuries or surgeries. Individuals with hemophilia may experience spontaneous bleeding episodes, particularly into joints and muscles. Other conditions, like von Willebrand disease, can also affect blood clotting but are distinct from hemophilia.