{
  "abstract": "Anomalous origin of the right coronary artery from the pulmonary artery (ARCAPA) is a rare congenital heart defect which can present through sudden death or asymptomatically in patients. There can be an association with coexistent cardiac defects, thus enforcing the importance of a structured full segmental sequential echocardiogram, and further imaging where coronaries appear unusually prominent without visible origin.",
  "authors": [
    {
      "affiliations": [
        "Division of Biomedical Sciences, St George’s University of London, London, UK"
      ],
      "name": "Simonette Carlton-Carew"
    },
    {
      "affiliations": [
        "King’s College London School of Medicine, London, UK"
      ],
      "name": "Minji Ho"
    },
    {
      "affiliations": [
        "St Thomas’ Hospital, London, UK"
      ],
      "name": "James Wong"
    },
    {
      "affiliations": [
        "Evelina London Children’s Healthcare, London, UK"
      ],
      "name": "Hannah Bellsham-Revell"
    }
  ],
  "title": "Diagnosis of anomalous origin of a right coronary artery from the pulmonary artery in the context of a suspected ventricular septal defect",
  "uid": "de783884-ca40-5c21-b389-e12cc64193c2"
}