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Familial hypofibrinolysis and venous thrombosis.

作者信息

Petäjä J, Rasi V, Myllylä G, Vahtera E, Hallman H

机构信息

Finnish Red Cross Blood Transfusion Service, Helsinki, Finland.

出版信息

Br J Haematol. 1989 Mar;71(3):393-8. doi: 10.1111/j.1365-2141.1989.tb04297.x.

Abstract

Nine patients with, and 11 without, venous thromboses (DVT) from two families were studied. In family 1, four members with, and one without, DVT had t-PA activity below the lower limit of the controls (21.3 IU/ml, n = 19) after 20 min venous occlusion (VO). After VO t-PA antigen (t-PA:Ag) was below the lowest value of the controls (22.8 ng/ml) in all five cases with low t-PA activity. All the family members, both with and without thrombosis, had normal t-PA inhibitor activities (PAI). In family 2 t-PA activity after VO was low in three symptomatic and four asymptomatic family members. t-PA:Ag was also low in four of these. PAI level was normal in all but one family member. Mild type I von Willebrand's disease was discovered in four members of family 2. Deficient t-PA:Ag response was found in two of these. Antithrombin III, protein C and protein S were normal in both families. It is concluded that low fibrinolytic capacity, independent of PAI, is associated with familial DVT. Our data suggests autosomal dominant inheritance.

摘要

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