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hemophilia A

Hemophilia A is a genetic disorder that affects the blood's ability to clot properly. It is caused by a deficiency in a specific protein called Factor VIII, essential for blood coagulation. People with hemophilia A experience prolonged bleeding after injuries or surgeries and may have spontaneous bleeding episodes, particularly into joints and muscles. This condition is usually inherited and mainly affects males. While there is no cure, management involves regular infusions of Factor VIII replacement therapy to help control bleeding and improve quality of life. Early diagnosis and treatment are crucial for effective management.

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  • Image for hemophilia A

    Hemophilia A is a genetic blood disorder where the body lacks sufficient clotting factor VIII, a protein essential for blood to clot properly. This deficiency leads to prolonged bleeding after injuries or surgery and can cause spontaneous bleeding episodes, especially in muscles and joints. It is usually inherited and more common in males. Treatment involves infusions of the missing clotting factor to help control bleeding and prevent complications. With proper care and management, individuals with hemophilia A can lead active and fulfilling lives, although they must be cautious to minimize injury and bleeding risks.