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Article

Myocardial infarction in a newborn heterozygous for the MTHFR C677T mutation.

Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society - 1 Jan 2000

Clark Amy B, Stokes Theophil A, Krous Henry F, Carbine Douglas N

Abstract excerpt

Neonatal myocardial infarction secondary to congenital heart disease, anomalous coronary artery anatomy, thromboembolism, coagulopathy, birth asphyxia, and unknown causes has been previously reported. We now report an infant who suffered a massive myocardial infarction during birth, requiring extensive resuscitation and aggressive management. A thrombus, the origin of which was not detected on autopsy, was found...

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Topics

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Share to Coronary Thrombosis
Share to MTHFR gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heterozygote

Share to Infant, Newborn

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Mutation

Share to Myocardial Infarction

Source

Identifiers

PMID: 22339112
DOI: 10.2350/11-09-1088-CR.1

Genes

MTHFR

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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