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1.
Int Angiol ; 22(2): 199-201, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12865888

ABSTRACT

We present the case of a 32-year-old man suffering from recurrent episodes of deep vein thrombosis (DVT). He was heterozygous for the G1691A mutation in the Factor V gene. His father was heterozygous for the same mutation and had a unique episode of DVT after a fracture of the tibia. Genetic predisposition significantly influences the prevalence of thrombotic events, however, additional unknown factors may be involved in the initiation and recurrence of venous thromboembolism.


Subject(s)
Popliteal Vein/pathology , Venous Thrombosis/diagnosis , Adult , Anticoagulants/therapeutic use , Greece , Heparin/therapeutic use , Humans , Male , Phlebography , Popliteal Vein/diagnostic imaging , Recurrence , Tomography, X-Ray Computed , Ultrasonography, Doppler, Duplex , Venous Thrombosis/drug therapy , Warfarin/therapeutic use
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