Acquired Factor X Deficiency in a Patient with Amyloidosis

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Abstract
A patient with extensive amyloidosis and a selective factor X deficiency is described. The following observations indicate that the factor X deficiency in this case is not inherited. 1. The first symptoms of a bleeding tendency appeared at an age of 50 years. 2. The patient’s four children had no clotting defect. 3. After infusion of 1 liter of fresh plasma no increased factor X activity was observed. No anticoagulants could be demonstrated in vitro.