Back to Search
Start Over
Thrombophilia in childhood: to test or not to test.
- Source :
-
Seminars in thrombosis and hemostasis [Semin Thromb Hemost] 2011 Oct; Vol. 37 (7), pp. 794-801. Date of Electronic Publication: 2011 Dec 20. - Publication Year :
- 2011
-
Abstract
- Inherited thrombophilia is defined as a genetically determined tendency to develop venous thromboembolism. In children, inherited thrombophilia contributes to the development of pediatric thromboembolic disease. As a consequence, pediatric hematologists are increasingly requested to test thrombophilia in pediatric patients with thrombosis or asymptomatic children from thrombophilic families. This article reviews the benefits and limitations of testing for thrombophilic disorders, for example, factor V Leiden, prothrombin mutation, and deficiencies of antithrombin, protein C, or protein S in childhood.<br /> (© Thieme Medical Publishers.)
- Subjects :
- Adolescent
Adult
Anticoagulants economics
Antithrombin III genetics
Antithrombin III Deficiency diagnosis
Antithrombin III Deficiency epidemiology
Child
Diagnostic Tests, Routine economics
Factor V genetics
False Positive Reactions
Female
Humans
Mutation
Pregnancy
Prevalence
Protein C genetics
Protein C Deficiency diagnosis
Protein C Deficiency epidemiology
Protein S genetics
Protein S Deficiency diagnosis
Protein S Deficiency epidemiology
Prothrombin genetics
Recurrence
Thrombophilia diagnosis
Thrombophilia genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1098-9064
- Volume :
- 37
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Seminars in thrombosis and hemostasis
- Publication Type :
- Academic Journal
- Accession number :
- 22187402
- Full Text :
- https://doi.org/10.1055/s-0031-1297170