Hemophilia is a medical condition in which the ability of the blood to clot is severely reduced causing the sufferer to bleed severely from even a slight injury.
There are four types of Hemophilia which are Hemophilia A-Also called classic hemophilia, it is four times more common than Hemophilia B, and it occurs when factor VIII levels are deficient, Hemophilia B-Also called christmas disease, it occurs when factor Xi levels are deficient, Hemophilia C-It occurs when facts of XI levels are deficient, and Acquired Hemophilia-is a rare autoimmune disorder characterized by bleeding that occurs in patients with a personal and family history negative for Hemorrhages.
Hemophilia affects males much more frequently 1 in 10,000 than females 1 in …show more content…
Until then they believed that the blood vessels of hemophiliacs were more fragile than none Hemophiliacs. In 1937, Patek and Taylor, two doctors at Harvard, found out they could correct the clotting problem by adding a substance which came from the plasma in blood. This was called hemophilic globulin. In 1944, pavlosky, a doctor from Buenos Aires, Argentina did a lab test which showed that blood from one hemophilic could correct the clotting problem in a second hemophilic. In 1952 there was a recognition of hemophilia A and hemophilia B as two distinct disease. As time goes by in the 1950s and early 1960s, hemophiliacs were treated whole blood or fresh plasma.
Most people with severe hemophilia and some people with mild or moderate hemophilia in childhood or early adulthood. Most of the time they died because they bled in very important organs like the brain, or bleeding after minor surgery or after an injury. Today ,there is still no cure but there is a treatment for hemophilia. The treatment for hemophilia is with blood transfusions and infusions of a blood derived substance antihemophilic factor. However, the treatment is very expensive and occasional problems can arise because of patient's allergic reactions or other transfer
There are four types of Hemophilia which are Hemophilia A-Also called classic hemophilia, it is four times more common than Hemophilia B, and it occurs when factor VIII levels are deficient, Hemophilia B-Also called christmas disease, it occurs when factor Xi levels are deficient, Hemophilia C-It occurs when facts of XI levels are deficient, and Acquired Hemophilia-is a rare autoimmune disorder characterized by bleeding that occurs in patients with a personal and family history negative for Hemorrhages.
Hemophilia affects males much more frequently 1 in 10,000 than females 1 in …show more content…
Until then they believed that the blood vessels of hemophiliacs were more fragile than none Hemophiliacs. In 1937, Patek and Taylor, two doctors at Harvard, found out they could correct the clotting problem by adding a substance which came from the plasma in blood. This was called hemophilic globulin. In 1944, pavlosky, a doctor from Buenos Aires, Argentina did a lab test which showed that blood from one hemophilic could correct the clotting problem in a second hemophilic. In 1952 there was a recognition of hemophilia A and hemophilia B as two distinct disease. As time goes by in the 1950s and early 1960s, hemophiliacs were treated whole blood or fresh plasma.
Most people with severe hemophilia and some people with mild or moderate hemophilia in childhood or early adulthood. Most of the time they died because they bled in very important organs like the brain, or bleeding after minor surgery or after an injury. Today ,there is still no cure but there is a treatment for hemophilia. The treatment for hemophilia is with blood transfusions and infusions of a blood derived substance antihemophilic factor. However, the treatment is very expensive and occasional problems can arise because of patient's allergic reactions or other transfer