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

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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Bibliographic Details
Main Authors: Leonardo G. P. Ruiz, Maria Gabriela L. Oliveira, Adriana L. Z. Ruiz, Camila S. Daher, Mauricio L. Nogueira
Format: Article
Language:English
Published: Sociedade Brasileira de Patologia Clínica 2018-04-01
Series:Jornal Brasileiro de Patologia e Medicina Laboratorial
Subjects:
thrombophilia
mutation
venous thrombosis
Online Access:http://www.scielo.br/pdf/jbpml/v54n2/1676-2444-jbpml-54-02-0092.pdf

Internet

http://www.scielo.br/pdf/jbpml/v54n2/1676-2444-jbpml-54-02-0092.pdf

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