20 top medical experts on Flaujeac factor deficiency across 3 countries, including 2 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Flaujeac factor deficiency: A rare genetic hematologic disease characterized by abnormal surface-mediated activation of fibrinolysis due to the deficiency of high-molecular-weight kininogen in plasma. Activated partial thromboplastin time (aPTT) may be prolonged. Clinically, patients are typically asymptomatic and do not show increased bleeding or thrombotic tendency.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Fitzgerald Trait,  HMWK Deficiency,  High molecular weight kininogen deficiency,  High Molecular Weight Kininogen Deficiency,  Total Kininogen Deficiency


  

        

                    


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