Factor X Deficiency and Systemic Amyloidosis
- 14 July 1977
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 297 (2) , 108-109
- https://doi.org/10.1056/nejm197707142970211
Abstract
The association of an isolated acquired factor X (Stuart-factor) deficiency and systemic acquired amyloidosis has been sporadically reported over the last 15 years,1 , 2 and over two thirds of the patients with acquired factor X deficiency have systemic amyloidosis. These facts suggest that an important relation exists between the two entities. In view of the isolated nature of the factor X deficiency it does not appear reasonable to implicate hepatocellular destruction by amyloid infiltrates as the causative mechanism, since most patients with acquired factor X deficiency have normal levels of other coagulation factors known to be of hepatocellular origin. In addition, . . .Keywords
This publication has 4 references indexed in Scilit:
- The isolation and identification of the P-component of normal human plasma proteins (Short Communication)Biochemical Journal, 1974
- Amyloidosis with factor X deficiencyThe Lancet Healthy Longevity, 1972
- Acquired Factor X Deficiency Associated with Systematized Amyloidosis—A Report of a CaseBlood, 1963