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Diffuse coronary artery dilatation in a neonate: a case report
R Parashar1, P J Lysecki, T Mondal
1Michael G. DeGroote School of Medicine, McMaster University, Hamilton, ON, Canada.
Journal of Neonatal-Perinatal Medicine
|November 20, 2013
Summary
A newborn experienced coronary artery dilatation without known causes, spontaneously recovering. This case suggests a potential early presentation of Kawasaki disease in neonates, even without typical symptoms.
Area of Science:
- Neonatal cardiology
- Pediatric infectious diseases
- Vascular inflammation
Background:
- Kawasaki disease is a leading cause of acquired heart disease in children.
- Neonatal presentation of Kawasaki disease is rare and often atypical.
- Coronary artery abnormalities are a hallmark of Kawasaki disease.
Observation:
- A neonate presented with diffuse, bilateral coronary artery dilatation on the first day of life.
- No intrauterine hypoxia or other causes for coronary ectasia were identified.
- The infant's symptoms resolved spontaneously without intervention.
Findings:
- The case presents a unique instance of spontaneous coronary artery dilatation in a neonate.
- This presentation challenges the typical diagnostic criteria for Kawasaki disease in newborns.
- The spontaneous resolution suggests a possible early or subclinical form of the disease.
Implications:
- This case highlights the importance of considering Kawasaki disease in neonates with unexplained coronary artery dilatation.
- Early recognition and treatment are crucial to prevent serious cardiac sequelae.
- Further research is needed to understand atypical Kawasaki disease presentations in neonates.

