What is Haemophilic factor?

What is Haemophilic factor?

People with hemophilia have low levels of either factor VIII (8) or factor IX (9). The severity of hemophilia that a person has is determined by the amount of factor in the blood. The lower the amount of the factor, the more likely it is that bleeding will occur which can lead to serious health problems.

Which clotting factor is anti Haemophilic globulin?

coagulation protein factor VIII (antihemophilic globulin). Of persons with hemophilia, approximately 85 percent have factor VIII deficiency. The next most common form of hemophilia, hemophilia B, is due to deficiency of factor IX (plasma thromboplastin component, or PTC).

What does a Haemophilic person lack?

Hemophilia is a rare disorder in which the blood doesn’t clot in the typical way because it doesn’t have enough blood-clotting proteins (clotting factors). If you have hemophilia, you might bleed for a longer time after an injury than you would if your blood clotted properly.

Does B12 cause blood clots?

Population research suggests that having low levels of vitamin B12 might be linked to an increased risk for blood clots in the veins.

What is acquired Factor VIII deficiency?

Acquired factor VIII deficiency is a bleeding disorder that requires prompt diagnosis and management to avert severe, life-threatening bleeding and death. Despite knowledge of this disorder of coagulation for several decades, relatively little is still known about this disease because of its rare incidence.

Which disease is known as Royal disease?

Hemophilia is sometimes referred to as “the royal disease,” because it affected the royal families of England, Germany, Russia and Spain in the 19th and 20th centuries.

What is Fletcher factor?

Prekallikrein (PK), also known as Fletcher factor, is an 85,000 Mr serine protease that complexes with high-molecular-weight kininogen. PK is the precursor of plasma kallikrein, which is a serine protease that activates kinins. PK is cleaved to produce kallikrein by activated Factor XII (Hageman factor).

What is the role of factor 12?

Factor XII (FXII) is a coagulation protein that is essential for surface-activated blood coagulation tests but whose deficiency is not associated with bleeding. For over forty years, investigators in hemostasis have not considered FXII important because its deficiency is not associated with bleeding.

What is the Christmas disease?

Hemophilia B, also known as factor IX deficiency or Christmas disease, is the second most common type of hemophilia. The disorder was first reported in the medical literature in 1952 in a patient with the name of Stephen Christmas.

What is antihemophilic factor (AHF)?

Antihemophilic factor (AHF) is a protein that is produced naturally in the body. It helps the blood form clots to stop bleeding and prevents bleeding problems from happening as often. Hemophilia A, also called classical hemophilia, is a condition where the body does not make enough AHF.

What is antihemophilic factor injection used for?

Antihemophilic factor (AHF) injection is used to treat and prevent serious bleeding episodes in patients with a bleeding problem called hemophilia A. The bleeding episode may be related to an injury (trauma) or a surgical procedure. AHF is a protein that is produced naturally in the body.

What is AHF hemophilia test?

Antihemophilia factor A test, AHF, factor VIII:C, coagulation factor test This test measures the activity of factor VIII, a blood-clotting protein. The test can find out whether you have hemophilia A or another clotting disorder. Hemophilia A is the most common severe bleeding disorder.

What is a lack of antihemophilic factor VIII?

A lack of antihemophilic factor VIII is the cause of hemophilia A. Human antihemophilic factor works by temporarily raising levels of factor VIII in the blood to aid in clotting. Human antihemophilic factor is used to treat or prevent bleeding episodes in people with hemophilia A.