Abstract |
Deep venous thrombosis (DVT) in children is more often associated with underlying pathological conditions than with hereditary thrombophilia. The present study is a retrospective analysis of thrombophilia in 285 pediatric patients with venous thrombosis at different sites. Four common thrombophilia markers, that is protein C, protein S, antithrombin III, and factor V Leiden (FVL) mutation, were analyzed. Thrombosis in hepatic and portal veins was more common in pediatric patients (73%) when compared to other sites (27%). Overall, hereditary thrombophilia accounted for 15.5% of the patients with venous thrombosis. The FVL mutation, which was the major causative factor in Budd-Chiari syndrome and portal vein thrombosis cases in the adult group, was not a major contributing factor in pediatric group, that is, 1.8% of the patients. In conclusion, the risk factors for venous thrombosis vary in different age groups.
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Authors | Navin Pai, Kanjaksha Ghosh, Shrimati Shetty |
Journal | Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
(Clin Appl Thromb Hemost)
Vol. 20
Issue 6
Pg. 573-6
(Sep 2014)
ISSN: 1938-2723 [Electronic] United States |
PMID | 23406614
(Publication Type: Clinical Trial, Journal Article)
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Copyright | © The Author(s) 2013. |
Chemical References |
- Biomarkers
- Protein C
- Protein S
- factor V Leiden
- Antithrombin III
- Factor V
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Topics |
- Adolescent
- Antithrombin III
(metabolism)
- Biomarkers
(blood)
- Budd-Chiari Syndrome
(blood, etiology, genetics)
- Child
- Child, Preschool
- Factor V
(genetics, metabolism)
- Female
- Humans
- India
- Infant
- Male
- Mutation
- Protein C
(metabolism)
- Protein S
(metabolism)
- Thrombophilia
(blood, complications, genetics)
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