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Combined heterozygosity of factor V Leiden and the G20210A prothrombin gene mutation in a patient with cerebral cortical vein thrombosis

  • Indiana University Bloomington
  • Riley Hospital for Children

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Cerebral venous thrombosis (CVT) is a rare type of stroke with a variety of causes. Several reports have suggested that either factor V Leiden or G20210A prothrombin gene mutation is associated with an increased risk of CVT. The genetic thrombophilias are typically associated with other predisposing factors. We report a unique case of CVT in a patient with both the factor V Leiden and the G20210A prothrombin gene mutations without other identifiable precipitating factors in a 28-year-old white male in good health. MRI and cerebral arterial angiography showed cerebral cortical venous thrombosis. This case suggests that combined heterozygous individuals may be particularly prone to spontaneous thrombosis, like CVT. (C) 2000 Wiley-Liss, Inc.

Original languageEnglish
Pages (from-to)226-228
Number of pages3
JournalAmerican Journal of Hematology
Volume64
Issue number3
DOIs
StatePublished - 2000

Keywords

  • Cerebral venous thrombosis
  • Factor V Leiden
  • Prothrombin gene mutation

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