Supraventricular tachyarrhythmia and sinus node dysfunction as a first manifestation of short QT syndrome in a pediatric patient. Case Report

Short QT syndrome (SQTS) represents a diagnosis challenge where the symptoms may vary from palpitations in an otherwise asymptomatic patient to sudden death. Is a recently discovered rare channelopathy, identified by Gussak in 2000, characterized by short QT intervals on the electrocardiogram and a...

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Veröffentlicht in:Journal of electrocardiology 2022-09, Vol.74, p.146-153
Hauptverfasser: Ploneda-Valencia, Ruy G., Ortiz-Solis, Willian A., Ruiz-Gonzalez, Gustavo, Santiago-Garcia, Ana K., Rivera-Rodríguez, Leonardo, Nava-Townsend, Santiago, Márquez, Manlio F., Levinstein-Jacinto, Moisés
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Sprache:eng
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Zusammenfassung:Short QT syndrome (SQTS) represents a diagnosis challenge where the symptoms may vary from palpitations in an otherwise asymptomatic patient to sudden death. Is a recently discovered rare channelopathy, identified by Gussak in 2000, characterized by short QT intervals on the electrocardiogram and a tendency to develop atrial and ventricular arrhythmias in the absence of structural heart disease, hyperkalemia, hypercalcemia, hyperthermia, acidosis and endocrine disorders. We present the case of a 16-year-old patient with short QT-type channelopathy, who presented with sinus arrest and junctional rhythm, who later developed atrial tachycardia and atrial flutter.
ISSN:0022-0736
1532-8430
DOI:10.1016/j.jelectrocard.2022.08.010