| Literature DB >> 21481934 |
Parham Eshtehardi1, Parisa Ghassemi-Kakroodi, Ali Garachemani, Masoud Eslami, Davood Akhlagh Moayed.
Abstract
We report on a 20-year-old man who presented with an extensive acute anteroseptal myocardial infarction (from a thrombotic occlusion of the left anterior coronary artery) as the initial manifestation of hereditary protein C deficiency. This case report, along with previous reports, indicates that a diagnosis of protein C deficiency in young patients with myocardial infarctions is essential for more appropriate management and for the prevention of recurrent events. Furthermore, family screening could lead to a prophylactic approach in carriers of this mutation.Entities:
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Year: 2011 PMID: 21481934 DOI: 10.1016/j.hrtlng.2010.07.015
Source DB: PubMed Journal: Heart Lung ISSN: 0147-9563 Impact factor: 2.210