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Thromb Haemost 1965; 13(02): 516-530
DOI: 10.1055/s-0038-1656297
Originalarbeiten — Original Articles — Travaux Originaux
Schattauer GmbH

Inherited Antithrombin Deficiency Causing Thrombophilia

O Egeberg
1   Institute for Thrombosis Research, Medical Department A, University Hospital, Rikshospitalet, Oslo, Norway. (Head: Prof. P.A. Owren, M. D.)
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Publication History

Publication Date:
27 June 2018 (online)

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Summary

Blood coagulation systems were studied in members of a family with remarkably high incidence of thrombo - embolic diseases. Thrombotic episodes most often occurred as deep venous thrombosis in the legs, with the first attack at the age of 10-25 years.

Pro coagulant factor activities were found within normal variation ranges.

Plasma antithrombin III (progressive antithrombin) activity was abnormally low in members with history of thrombosis and in some of their children, with an average level of about 50 per cent of normal.

Heparin resistance measured with plasma heparin thrombin time was increased in members with low antithrombin III, and plasma heparin cofactor activity was decreased.

The results strongly support the explanation that antithrombin III and heparin cofactor are one and the same plasma substance, and that deficiency of this antithrombin can cause a severe tendency to thrombosis.

The antithrombin deficiency seems to be inherited as an autosomal dominant trait.

 

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