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What is haemophilia in health sciences?

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Haemophilia is a rare condition that is inherited  affecting clotting factors making it difficult to stop bleeding and can lead to death.
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Haemophilia is a genetic disorder that affects the blood's ability to clot, leading to excessive bleeding and a higher risk of injury-related bleeding episodes. It is caused by a deficiency in specific clotting proteins, either Factor VIII (Haemophilia A) or Factor IX (Haemophilia B).

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It's bleeding disorder that can turn a simple bump or scrape into major headache. You see, haemophilia affects the way our blood clots, which is kind of like the body's own a little band-aid. The haemophilia, the body doesn't make enough protein called clotting factor, which means that cuts and injuries can leads to excessive bleeding. It can be real pain in the joint, leading the swelling and stiffness, especially in the knees, elbows and ankles.
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Haemophilia is a rare genetic bleeding disorder in which the blood doesn't clot normally due to a deficiency or dysfunction of specific blood clotting proteins (clotting factors). This can cause spontaneous bleeding episodes, prolonged bleeding after injury or surgery, and increased risk of bleeding in joints and muscles. There are two main types of haemophilia: Hemophilia A (factor VIII deficiency) and Hemophilia B (factor IX deficiency).
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Haemophilia is a genetic bleeding disorder that affects the ability of the blood to clot. It is caused by a deficiency or absence of certain clotting factors in the blood, which are essential for normal blood clotting. Haemophilia is classified into two types, haemophilia A and haemophilia B, depending on the specific clotting factor that is deficient. Haemophilia A is caused by a deficiency of clotting factor VIII, while haemophilia B is caused by a deficiency of clotting factor IX. People with haemophilia are at risk for excessive bleeding and bruising, even from minor injuries. They may also experience spontaneous bleeding episodes, particularly into the joints, which can cause pain, swelling, and limited range of motion. Haemophilia is a lifelong condition that requires careful management and regular monitoring. Treatment typically involves replacement therapy with clotting factors, which can be administered through injections or infusions. In some cases, gene therapy may be used to treat haemophilia by introducing a functional copy of the missing clotting factor gene into the patient's cells. Haemophilia is a rare condition that affects approximately 1 in 10,000 people worldwide. It is typically inherited in an X-linked recessive pattern, which means that it is passed down from mothers to their sons.
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This is inherited bleeding disorder in which the blood does not clot properly, this can lead to spontaneous bleeding as well as from the injures or surgery
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Haemophilia is a genetic disorder that affects the body's ability to form blood clots, which can lead to excessive bleeding and bruising. The condition is caused by a deficiency or absence of clotting factors in the blood, which are proteins that help the blood clot and stop bleeding.

There are two main types of haemophilia: haemophilia A, which is caused by a deficiency of clotting factor VIII, and haemophilia B, which is caused by a deficiency of clotting factor IX. Both types are inherited in an X-linked recessive manner, which means that the condition primarily affects males and is passed down from carrier females.

Symptoms of haemophilia can include excessive bleeding following injury or surgery, frequent nosebleeds, and easy bruising. In severe cases, spontaneous bleeding into joints and muscles can occur, which can lead to chronic pain and joint damage.

Treatment for haemophilia typically involves replacing the missing clotting factor through intravenous infusions of clotting factor concentrates. Prophylactic treatment can also be used to prevent bleeding episodes and reduce the risk of joint damage
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Haemophilia is a rare genetic disorder that affects the body's ability to control blood clotting. People with haemophilia are at risk of excessive bleeding, even from minor injuries. Haemophilia is caused by a deficiency in one of the proteins needed for normal blood clotting. Treatment for haemophilia usually involves replacing the missing protein to help the blood clot properly. In some cases, surgery may also be necessary to stop bleeding.
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The haemophilia, the body doesn't make enough protein called clotting factor, which means that cuts and injuries can leads to excessive bleeding. It can be real pain in the joint, leading the swelling and stiffness, especially in the knees, elbows and ankles.
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