Coagulation defects
- condition in which there is a deviation from or interruption of the normal coagulation properties of the blood.
- A condition in which there is a deviation from or interruption of the normal coagulation properties of the blood.
Congenital factor viii disorder
- classic hemophilia resulting from a deficiency of factor VIII; an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.
- An inherited deficiency of coagulation Factor VIII characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage. Inherited as an x-linked recessive disease, hemophilia A is the most common hemophilia, occurring in approximately 1 in 10,000 male births. --2004
- Group of hereditary disorders in which affected individuals fail to make enough of certain proteins needed to form blood clots.
- A deficiency or abnormality of a blood coagulation factor characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage, Hemophilia is typically a hereditary disorder but, rarely, may be acquired. Inherited coagulation factor-deficient hemophilias include hemophilia A or classic hemophilia (Factor VIII deficiency) hemophilia B or Christmas disease (Factor IX deficiency), and hemophilia C (Factor XI deficiency). In individuals without hereditary hemophilia A, Factor VIII inhibitors may occur spontaneously as autoantibodies, resulting in a condition known as 'acquired hemophilia.' Approximately 10 % of patients with acquired hemophilia have an underlying malignancy. --2004
Congenital factor ix disorder
- deficiency of blood coagulation factor IX inherited as an X-linked disorder; clinical features resemble those in hemophilia A, but patients present with fewer symptoms.
Congenital factor xi deficiency
Congenital deficiency of other clotting factors
- deficiency or absence of fibrinogen (coagulation factor I) in the blood.
- absence or reduced levels of prothrombin in the blood.
Von willebrand's disease
- hemophilioid disorder due to deficiency of Von Willebrand factor and thus of Factor VIII complex.
Hemorrhagic disorder due to intrinsic circulating anticoagulants
Defibrination syndrome
- disorder characterized by reduction in the elements involved in blood coagulation due to their utilization in widespread blood clotting within the vessels; the activation of the clotting mechanism may arise from any of a number of disorders; in the late stages, it is marked by profuse hemorrhaging.
- A disorder characterized by reduction in the elements involved in blood coagulation due to their utilization in widespread blood clotting within the vessels.
- A pathological process in the body where the blood starts to coagulate throughout the whole body. This depletes the body of its platelets and coagulation factors, and there is an increased the risk of hemorrhage.
Acquired coagulation factor deficiency
Other and unspecified coagulation defects
- condition in which there is a deviation from or interruption of the normal coagulation properties of the blood.
- A condition in which there is a deviation from or interruption of the normal coagulation properties of the blood.
