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Article

Acute myocardial infarction with large bilateral intracoronary thrombi in a young patient with the prothrombin 20210 G-->A mutation.

Catheterization and cardiovascular diagnosis - 1 Aug 1998

de Winter R J, Middeldorp S, Gaffar S, Koch K T, Piek J J, Levi M, Reitsma P H

Abstract excerpt

A genetic variation in the 3'-UT region of the prothrombin gene, a G to A mutation at nucleotide 20210, has been associated recently with increased risk of acute myocardial infarction. We describe a case of a young patient carrying the mutation, with an AMI caused by large bilateral intracoronary...

Topics

Adult
Base Sequence
Coronary Angiography
Coronary Thrombosis
DNA Mutational Analysis
Electrocardiography
Genetic Carrier Screening
Genetic Variation
Humans
Male
Myocardial Infarction

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Nucleotide Mapping

Pedigree

Prothrombin

Thrombophilia

Source

Identifiers

PMID: 9716211
DOI: 10.1002/(sici)1097-0304(199808)44:4<427::aid-ccd15>3.0.co;2-f

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9716211-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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Acute myocardial infarction with large bilateral intracoronary thrombi in a young patient with the prothrombin 20210 G-->A mutation.PMID 9716211Read ↗

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Interaction of coagulation defects and cardiovascular risk factors: increased risk of myocardial infarction associated with factor V Leiden or prothrombin 20210A.Semantic proximity Read ↗

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The 20210 G → A mutation in the 3′‐untranslated region of the prothrombin gene and the risk for arterial thrombotic diseaseSemantic proximity Read ↗

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