Abstract |
Important recent advances in the field of the biology of recurrent venous thrombosis include greater understanding of congenital deficiency states involving antithrombin III (AT III) and protein C. Other disturbances demonstrated were related to fibrinolysis frequently, and rarely platelet function and coagulation factors. Possible existence of these anomalies requires investigation during biologic tests in cases of recurrent venous thrombosis, particularly in the presence of a family history or onset of the initial affection before 40 years of age. Confirmation of the importance of screening for such anomalies is supplied by results of a study of 11 families with antithrombin III deficiency and 9 families deficients in protein C, and a literature review of cases. However, currently available biologic tests provide data enabling only partial explanation of the mechanism underlying recurrent venous thrombosis accidents.
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Authors | M Samama, J Conard, M H Horellou, A Veuillet-Duval, J J Lefrére |
Journal | Journal des maladies vasculaires
(J Mal Vasc)
Vol. 9
Issue 4
Pg. 321-5
( 1984)
ISSN: 0398-0499 [Print] France |
Vernacular Title | Biologie des thromboses veineuses récidivantes. |
PMID | 6549340
(Publication Type: English Abstract, Journal Article)
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Chemical References |
- Blood Coagulation Factors
- Glycoproteins
- Protein C
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Topics |
- Antithrombin III Deficiency
- Blood Coagulation Factors
(physiology)
- Blood Platelets
(physiology)
- Fibrinolysis
- Glycoproteins
(deficiency)
- Humans
- Protein C
- Recurrence
- Thrombophlebitis
(genetics, physiopathology)
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