Hemophilia
Hemophilia is a genetic disorder that affects the blood's ability to clot, leading to excessive bleeding from injuries or even spontaneously. It is caused by a deficiency in specific clotting factors, proteins necessary for blood to clot properly. The condition is primarily inherited and more common in males. People with hemophilia may have to manage their condition with medications, such as clotting factor replacements, and take precautions to prevent injuries. While there is no cure, appropriate treatment allows many individuals to lead active lives. Regular medical care is essential for managing the condition effectively.
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Hemophilia is a genetic disorder that affects the blood's ability to clot, leading to prolonged bleeding after injuries or surgeries. This condition is primarily caused by a deficiency in specific proteins called clotting factors, which are essential for the blood clotting process. Hemophilia is usually inherited, affecting mostly males, while females can be carriers. There are different types, with hemophilia A and B being the most common. People with hemophilia may require treatments, including replacement therapy with clotting factors, to manage their condition and prevent or treat bleeding episodes.