ArticleCase reports in pediatrics2025
Diagnosis of a Neonate With Long QT Syndrome and Severe Complications Delayed due to an Unrecognized Familial History.
Article in Case reports in pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Long QT syndrome (LQTS) is a hereditary arrhythmic disorder associated with sudden cardiac death. We report a neonatal case of congenital LQTS that went undiagnosed in utero, leading to severe postnatal complications. A male preterm infant was delivered by emergency cesarean section due to fetal hydrops. Shortly after birth, he developed respiratory failure and metabolic acidosis, followed by ventricular tachycardia and torsades de pointes requiring prolonged resuscitation. During cardiopulmonary resuscitation, the father collapsed, and it was subsequently established that he had been receiving treatment for LQTS. The paternal grandmother also had the same diagnosis. Genetic testing performed for the infant identified a pathogenic
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