Stunna
Valued Contributor
Hemophilia is a genetic disorder that affects the blood's ability to clot properly. It is caused by a deficiency or absence of certain blood clotting factors, most commonly factor VIII (8) or factor IX (9). As a result, people with hemophilia may experience prolonged bleeding after injury or surgery, as well as spontaneous bleeding into muscles and joints.
Hemophilia is usually inherited in an X-linked recessive pattern, which means that it primarily affects males. Females are typically carriers of the condition and can pass it on to their children. However, in rare cases, females can also develop hemophilia if they inherit two copies of the mutated gene, one from each parent.
There are different types of hemophilia, including hemophilia A (factor VIII deficiency), hemophilia B (factor IX deficiency), and hemophilia C (factor XI deficiency). The severity of the condition can also vary depending on the amount of clotting factor that is missing or deficient.
Hemophilia is a lifelong condition that requires ongoing management, including regular infusions of clotting factor to prevent bleeding episodes. With proper treatment and care, people with hemophilia can lead full and active lives..
The symptoms of hemophilia can vary depending on the severity of the condition. People with mild hemophilia may not experience any symptoms unless they undergo surgery or experience a significant injury. However, people with moderate or severe hemophilia may experience frequent and prolonged bleeding, both internally and externally.
Hemophilia is usually inherited in an X-linked recessive pattern, which means that it primarily affects males. Females are typically carriers of the condition and can pass it on to their children. However, in rare cases, females can also develop hemophilia if they inherit two copies of the mutated gene, one from each parent.
There are different types of hemophilia, including hemophilia A (factor VIII deficiency), hemophilia B (factor IX deficiency), and hemophilia C (factor XI deficiency). The severity of the condition can also vary depending on the amount of clotting factor that is missing or deficient.
Hemophilia is a lifelong condition that requires ongoing management, including regular infusions of clotting factor to prevent bleeding episodes. With proper treatment and care, people with hemophilia can lead full and active lives..
The symptoms of hemophilia can vary depending on the severity of the condition. People with mild hemophilia may not experience any symptoms unless they undergo surgery or experience a significant injury. However, people with moderate or severe hemophilia may experience frequent and prolonged bleeding, both internally and externally.