Table 1.

Clinical characteristics and laboratory data of the family members

ParticipantSexAge, yThrombotic eventsAge at first VTE, yPT/INRaPTT, s*FVIII:C, %FVIII:Ag, %VWF:Ag, %§Additional thrombophilic defects
Family A           
 II-3, proband 53 DVT and PE 31 2.88 26.5 422 432 165 No 
 I-4 77 DVT and PE 49 1.00 21.6 269 296 144 No 
 II-6 45 SVT and DVT 43 0.98 21.1 416 372 60 No 
 III-1 26 No — 1.11 29.3 132 152 144 No 
 III-2 22 No — 1.1 27.2 323 368 112 No 
Family B           
 II-1, proband 41 DVT and PE 21 3.1 40 264 273 78 Heterozygous FV Leiden 
 I-2 66 DVT 24 0.93 22.2 508 457 68 Heterozygous FV Leiden 
 III-1 19 No — 1.07 26.2 295 270 113 Heterozygous FV Leiden 
ParticipantSexAge, yThrombotic eventsAge at first VTE, yPT/INRaPTT, s*FVIII:C, %FVIII:Ag, %VWF:Ag, %§Additional thrombophilic defects
Family A           
 II-3, proband 53 DVT and PE 31 2.88 26.5 422 432 165 No 
 I-4 77 DVT and PE 49 1.00 21.6 269 296 144 No 
 II-6 45 SVT and DVT 43 0.98 21.1 416 372 60 No 
 III-1 26 No — 1.11 29.3 132 152 144 No 
 III-2 22 No — 1.1 27.2 323 368 112 No 
Family B           
 II-1, proband 41 DVT and PE 21 3.1 40 264 273 78 Heterozygous FV Leiden 
 I-2 66 DVT 24 0.93 22.2 508 457 68 Heterozygous FV Leiden 
 III-1 19 No — 1.07 26.2 295 270 113 Heterozygous FV Leiden 

Participants are coded as in Figure 1.

INR, international normalized ratio; PT, prothrombin time; SVT, superficial vein thrombosis.

*

Normal range, 26 to 34 seconds.

Normal range, 58% to 162%.

Normal range, 64% to 156%.

§

Normal range, 52% to 178%.

Age at death.

Oral anticoagulant treatment (warfarin).

Close Modal

or Create an Account

Close Modal
Close Modal