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Factor XII (Hageman factor) deficiencyDefinitionThis is an inherited disorder with no symptoms. It does not cause abnormal bleeding in the affected person, but the blood takes longer than normal to clot (coagulate) in a test tube. It results from a deficiency of the plasma protein factor XII. CausesFactor XII deficiency is a rare hereditary disorder that is usually found when clotting tests are done for routine screening. It is not associated with abnormal bleeding. SymptomsThere are usually no symptoms. Exams and Tests
TreatmentTreatment is generally unnecessary. Outlook (Prognosis)The outcome is expected to be good without treatment. Possible ComplicationsThere are usually no complications. When to Contact a Medical ProfessionalThis condition is usually discovered by the health care provider when prolonged clotting is noticed in the process of running other laboratory tests. PreventionThis is an inherited disorder. There is no known way to prevent it.
Review Date:
4/15/2005 Reviewed By: Rita Nanda, MD, Department of Medicine, Section of Hematology/Oncology, University of Chicago Medical Center, Chicago, IL. Review provided by VeriMed Healthcare Network. The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. © 1997-
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