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Hereditary thrombophilia by factor V Leiden G1691A (heterozygous) and FII prothrombin G20210A (homozygous) mutations in a patient with ischemic cerebrovascular accident

ABSTRACT Mutations related to Factor V Leiden (G1691A) and prothrombin (G20210A) are associated with a significantly increased risk of venous thromboembolism. The identification of a patient affected by episodes of venous thromboembolism and carrier of G1691A (heterozygous) and G20210A (homozygous)...

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Main Authors: Leonardo G. P. Ruiz (Author), Maria Gabriela L. Oliveira (Author), Adriana L. Z. Ruiz (Author), Camila S. Daher (Author), Mauricio L. Nogueira (Author)
Format: Book
Published: Sociedade Brasileira de Patologia Clínica, 2018-04-01T00:00:00Z.
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Summary:ABSTRACT Mutations related to Factor V Leiden (G1691A) and prothrombin (G20210A) are associated with a significantly increased risk of venous thromboembolism. The identification of a patient affected by episodes of venous thromboembolism and carrier of G1691A (heterozygous) and G20210A (homozygous) polymorphisms was determined by molecular tests [real-time polymerase chain reaction (PCR) methodology, Genexpert system] during attendance at the Base Hospital of São José do Rio Preto-SP, Brazil.
Item Description:1678-4774
10.5935/1676-2444.20180016

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