TRANSIENT HYPERTROPHIC CARDIOMYOPATHY IN AN INFANT OF A DIABETIC MOTHER: CLINICAL CASE
DOI:
https://doi.org/10.52340/jecm.2026.03.06Keywords:
hypertrophic cardiomyopathy, infant, diabetic mother, echocardiographyAbstract
Introduction: Hypertrophic cardiomyopathy (HCM) is a common inherited cardiomyopathy characterized by left ventricular hypertrophy, with an annual pediatric incidence of 0.3–0.5 per 100,000. A distinct subset is transient HCM in infants of diabetic mothers (IDMs), seen echocardiographically in 13–44% of such infants, symptomatic in up to 12.1%.
Case: A male neonate born at 36 6/7 weeks to a mother with insulin-dependent type 2 diabetes and pre-eclampsia developed respiratory distress at birth. Echocardiography showed biventricular hypertrophy with predominant septal thickening (IVSD 0.92 cm), preserved EF (75%), and no outflow obstruction. He was discharged stable on day 11. At one month, repeat echocardiography showed marked regression (IVSD 0.4 cm, EF 81%) without pharmacologic therapy.
Conclusion: Transient HCM in IDMs is a self-limited, hyperinsulinemia-driven condition. Early echocardiographic screening and serial monitoring are essential to distinguish it from genetic HCM and guide management.
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References
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