A case report of myocardial infarction in young patient with a parental history of premature cardiovascular death: Combination of prothrombotic gene mutations (Articolo in rivista)

Type
Label
  • A case report of myocardial infarction in young patient with a parental history of premature cardiovascular death: Combination of prothrombotic gene mutations (Articolo in rivista) (literal)
Anno
  • 2008-01-01T00:00:00+01:00 (literal)
Alternative label
  • Botto N.; Mariani M.; Manfredi S.; Andreassi M. G. (2008)
    A case report of myocardial infarction in young patient with a parental history of premature cardiovascular death: Combination of prothrombotic gene mutations
    in International journal of cardiology (print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Botto N.; Mariani M.; Manfredi S.; Andreassi M. G. (literal)
Pagina inizio
  • e17 (literal)
Pagina fine
  • e19 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 130 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#note
  • In: International Journal of Cardiology, vol. 130 (1) pp. e17 - e19. Elsevier, 2008. (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • CNR-Institute of Clinical Physiology and Fondazione Gabriele Monasterio (literal)
Titolo
  • A case report of myocardial infarction in young patient with a parental history of premature cardiovascular death: Combination of prothrombotic gene mutations (literal)
Abstract
  • We report a case ofmyocardial infarction at a young age in a subject heterozygous for the G20210A prothrombin gene variant and homozygous for the C677TMTHFR polymorphism, who presented a strong family history of atherothrombosis. Genetic screening for inherited thrombophilia, especially in the presence of a strong familiarity, may be a critical information for secondary prevention of arterial thrombosis. (literal)
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