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Published on: June 2, 2015
Acquired and Heritable Thrombophilia in Indian Patients With Pediatric Deep Venous Thrombosis (DVT)
Navin Pai1, Kanjaksha Ghosh1, Shrimati Shetty2
1National Institute of Immunohaematology (ICMR), KEM Hospital, Mumbai, India.
Insights
Pediatric deep venous thrombosis (DVT) often stems from other health issues, not primarily hereditary thrombophilia. Factor V Leiden mutation is less common in children compared to adults.
Area of Science:
- Pediatric Hematology
- Vascular Medicine
- Genetics
Background:
- Deep venous thrombosis (DVT) in children presents unique etiological factors.
- Underlying pathological conditions are frequently implicated in pediatric venous thromboembolism.
- Hereditary thrombophilia plays a variable role across different age groups.
Purpose of the Study:
- To analyze the prevalence and type of thrombophilia in pediatric patients with venous thrombosis.
- To compare thrombophilia markers and thrombosis sites in children.
- To identify risk factors for venous thrombosis in pediatric populations.
Main Methods:
- Retrospective analysis of 285 pediatric patients diagnosed with venous thrombosis.
- Assessment of four common thrombophilia markers: protein C, protein S, antithrombin III, and factor V Leiden (FVL) mutation.
- Categorization of thrombosis based on anatomical site.
Main Results:
- Hepatic and portal vein thrombosis occurred in 73% of pediatric cases.
- Hereditary thrombophilia was identified in 15.5% of the pediatric cohort.
- Factor V Leiden mutation was found in only 1.8% of pediatric patients, unlike its higher prevalence in adult thrombosis.
Conclusions:
- Venous thrombosis risk factors differ significantly between pediatric and adult populations.
- Underlying conditions are more significant drivers of DVT in children than hereditary thrombophilia.
- Factor V Leiden mutation is not a primary contributor to pediatric venous thrombosis.
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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