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Definition
Factor VII deficiency is an inherited disorder in which a lack (deficiency) of plasma protein factor VII leads to abnormal bleeding.
Alternative Names
Extrinsic factor deficiency
Causes, incidence, and risk factors
This disorder occurs when the body does not have enough factor VII, an important blood clotting protein.
When you bleed, the body launches a series of reactions that help the blood clot. The process involves special proteins called coagulation factors. Factor VII is one of many coagulation factors. The final product of these reactions is the blood clot.
When certain coagulation factors are missing, your blood may not clot normally and you can bleed abnormally. Bleeding can vary from mild to severe in the same person over time. Bleeding may begin during infancy or childhood.
Most often a deficiency of factor VII is caused by:
- Severe liver disease
- Use of drugs that prevent clotting (anticoagulants such as warfarin or coumadin)
- Lack of vitamin K due to long-term use of antibiotics, bile duct obstruction, or poor absorption of vitamin K from the intestines
Some babies are born with vitamin K deficiency. It is very rare to be born with factor VII deficiency that is due to the body's inability to make working factor VII.
Symptoms
- Bleeding from mucus membranes
- Bleeding into joints
- Bleeding into muscles
- Excessive bruising
- Excessive menstrual bleeding
- Nosebleeds (epistaxis)
Signs and tests
Treatment
Patients can control bleeding episodes by receiving normal plasma, concentrates of factor VII, or genetically produced (recombinant) factor VII through a vein (intravenous). People need frequent treatment during bleeding episodes because factor VII does not last for long inside the body.
Women can better control menstrual bleeding with oral birth control (contraceptives). A form of factor VII called Novo-7 can also be used.
If a lack of vitamin K is causing the disorder, you can take vitamin K by mouth, through injections under the skin, or intravenously.
Support Groups
You can often help the stress of illness by joining a support group where members share common experiences and problems. See hemophilia - resources.
Reviewer Info: David C. Dugdale, III, MD, Professor of Medicine, Division of General Medicine, Department of Medicine, University of Washington School of Medicine; and Yi-Bin Chen, MD, Leukemia/Bone Marrow Transplant Program, Massachusetts General Hospital. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc., 03/02/2009



