Abstract
A 2-year-old girl with tetralogy of Fallot presented with diffuse cranial infarct after cardiac angiography. Heterozygosity for factor V Leiden and prothrombin 20210A mutations were detected. The authors suggest that if thrombosis develops in patients with congenital heart disease, genetic risk factors should be evaluated. © 2009, SAGE Publications. All rights reserved.
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Sipahi, T., Karademir, S., Kuybulu, A., & Akar, N. (2009). Diffuse Cerebral Infarct Associated With Factor V Leiden and Prothrombin 20210A Mutations in a Patient With Tetralogy of Fallot. Clinical and Applied Thrombosis/Hemostasis, 15(6), 705–707. https://doi.org/10.1177/1076029608319883
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