Prothrombin G20210A mutation in a child with spinal cord infarction.
case_report · Level V
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- Record sourced from PubMed, PMID 10356151.
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Abstract
Prothrombin G20210A is a newly described common mutation that is associated with an increased risk of arterial and venous thrombosis. We describe a healthy child heterozygous for this prothrombin mutation who had a spinal cord infarct with no other prothrombotic risk factors.
Medical subject headings
- Infarction
- Mutation
- Prothrombin
- Spinal Cord