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Published on: May 24, 2016
A unique case of reversible myocardial ischemia in a hyperthyroid neonate
Christina Trapali1, Heracles D Dellagrammaticas, Angeliki Nika
1Department of Cardiology, University of Athens, P. and A. Kyriakou Children's Hospital, Athens, Greece.
Insights
Neonatal hyperthyroidism can cause severe cardiac issues like heart failure and myocardial ischemia. Prompt treatment with beta-blockers and propylthiouracil successfully reversed these abnormalities in an infant.
Area of Science:
- Neonatal cardiology
- Pediatric endocrinology
- Maternal-fetal medicine
Background:
- Neonatal hyperthyroidism is rare but can lead to significant cardiovascular complications.
- Maternal hyperthyroidism can impact fetal and neonatal well-being, though diagnosis in the neonate preceding the mother is unusual.
Observation:
- An 8-day-old preterm neonate presented with heart failure, pulmonary hypertension, and myocardial ischemia.
- These cardiac abnormalities were attributed to untreated hyperthyroidism.
Findings:
- Treatment with beta-blockers and subsequently propylthiouracil led to the reversal of all cardiac abnormalities.
- The mother was diagnosed with hyperthyroidism after her infant's diagnosis, a reversal of the typical diagnostic sequence.
Implications:
- This case highlights the importance of considering neonatal hyperthyroidism in infants with unexplained cardiac dysfunction.
- Early diagnosis and treatment can prevent long-term sequelae, as evidenced by the child's normal 10-year follow-up.
- The successful management of ischemic abnormalities in a neonate due to hyperthyroidism has not been previously reported.
Abstract:
A case of an 8-day-old preterm neonate with heart failure, pulmonary hypertension, and myocardial ischemia due to hyperthyroidism is reported. Treatment of the disease initially with b-blockers and, upon establishment of hyperthyroidism, with propylthiouracil reversed all cardiac abnormalities. Contrary to the rule, diagnosis of hyperthyroidism in the mother was established following the diagnosis of the condition in her baby. On long-term follow-up (10 years), the child has developed normally, remains euthyroid with normal electrocardiogram. To our knowledge, diagnosis and reversal of the above-mentioned ischemic abnormalities have not been previously reported in neonates.
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