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Age-specific onset and distribution of the natural anticoagulant deficiency in pediatric thromboembolism
Age-specific onset and distribution of the natural anticoagulant deficiency in pediatric thromboembolism
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Age-specific onset and distribution of the natural anticoagulant deficiency in pediatric thromboembolism
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Age-specific onset and distribution of the natural anticoagulant deficiency in pediatric thromboembolism
Age-specific onset and distribution of the natural anticoagulant deficiency in pediatric thromboembolism

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Age-specific onset and distribution of the natural anticoagulant deficiency in pediatric thromboembolism
Age-specific onset and distribution of the natural anticoagulant deficiency in pediatric thromboembolism
Journal Article

Age-specific onset and distribution of the natural anticoagulant deficiency in pediatric thromboembolism

2016
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Overview
Background: The early diagnosis of inherited thrombophilia in children is challenging because of the rarity and hemostatic maturation. Methods: We explored protein C (PC), protein S (PS), and antithrombin (AT) deficiencies in 306 thromboembolic patients aged ≤20 y using the screening of plasma activity and genetic analysis. Results: Reduced activities were determined in 122 patients (40%). Low PC patients were most frequently found in the lowest age group (0–2 y, 45%), while low PS or low AT patients were found in the highest age group (16–20 y; PS: 30% and AT: 20%). Genetic study was completed in 62 patients having no other causes of thromboembolism. Mutations were determined in 18 patients (8 PC, 8 PS, and 2 AT genes). Six of eight patients with PC gene mutation were found in age 0–2 y (75%), while six of eight patients with PS gene mutation were in 7–20 y. Two AT gene–mutated patients were older than 4 y. Four PC-deficient and two PS-deficient patients carried compound heterozygous mutations. All but one PC gene–mutated patient suffered from intracranial thromboembolism, while PS/AT gene–mutated patients mostly developed extracranial venous thromboembolism. Conclusion: Stroke in low PC infants and deep vein thrombosis in low PS/AT school age children could be targeted for genetic screening of pediatric thrombophilias.