Hemophilia
This condition is called hemophilia.
Haemophilia A - an inhibition of clotting caused by a deficiency in a protein called Clotting Factor VIII Haemophilia B - an inhibition of clotting caused by a deficiency in a protein called Clotting Factor IX Haemophilia C - an inhibition of clotting caused by a deficiency in a protein called Clotting Factor XI -similar to- vonWillebrand's Disorder - an inhibition of clotting caused by a deficiency in a protein called the vonWillebrand's Factor
Medical practitioners diagnose clotting deficiency by conducting blood clotting tests.
Blood clotting
Thrombocytopenia is the medical term that refers to a deficiency of clotting cells, specifically platelets, in the blood. It can lead to abnormal bleeding and bruising due to the decreased ability of the blood to clot properly.
Thrombocytopenia is the medical term meaning a deficiency of clotting cells. -penia is the combining form meaning deficiency.
All hemophilia sufferers have a deficiency in clotting factors, which are proteins needed to form blood clots and stop bleeding. This deficiency makes them prone to prolonged bleeding episodes even from minor injuries. Hemophilia is typically an inherited disorder caused by mutations in specific genes.
The main cause of a longer clotting time is the deficiency of the clotting factor in the blood. This is as a result of a damaged platelet in the blood cells.
Hemophilia is caused by a deficiency of clotting factor VIII (hemophilia A) or clotting factor IX (hemophilia B).
Hemophilia is a genetic disorder caused by a deficiency or defect in clotting factor VIII (hemophilia A) or factor IX (hemophilia B). These clotting factors are essential for blood clot formation, and their deficiency leads to prolonged bleeding and poor clotting ability.
The prognosis for correcting vitamin K deficiency, and associated blood-clotting problems, is excellent.
Hemophilia is a bleeding disorder that slows down the blood clotting process. People who have hemophilia often have longer bleeding after an injury or surgery. People who have severe hemophilia have spontaneous bleeding into the joints and muscles. Hemophilia occurs more commonly in males than in females.The two most common types of hemophilia are hemophilia A (also known as classic hemophilia) and hemophilia B (also known as Christmas disease). People who have hemophilia A have low levels of a blood clotting factor called factor eight (FVIII). People who have hemophilia B have low levels of factor nine (FIX).The two types of hemophilia are caused by permanent gene changes (mutations) in different genes.