Factor XII (Hageman factor) deficiency

This is an inherited disorder that causes prolonged clotting (coagulation) of blood in a test tube without a clinical bleeding tendency, and results from a deficiency of the plasma protein factor XII.

Causes, incidence, and risk factors

Factor XII deficiency is a hereditary disorder that is usually found when clotting tests are done for routine screening. It is not associated with abnormal bleeding , and is a rare disorder.

Signs and tests

  • Prolonged
  • partial thromboplastin time
  • Abnormal
  • Factor XII assay

    Treatment

    Treatment is generally unnecessary.

    Expectations (prognosis)

    The outcome is expected to be good, even without treatment.

    Complications

    There are usually no complications.

    Calling your health care provider

    This condition is usually discovered by the health care provider when prolonged clotting is noticed in the process of running other laboratory tests.

    Prevention

    This is an inherited disorder. There is no known way to prevent it.

    Treatment Options – Sorted by Soonest Available

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