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Long QT Syndrome-2 (LQT2) is a rare congenital disorder of ventricular myocardial repolarization due to heterozygous mutations in the alpha subunit of the rapid rectifier potassium channel of HERG and… Click to show full abstract
Long QT Syndrome-2 (LQT2) is a rare congenital disorder of ventricular myocardial repolarization due to heterozygous mutations in the alpha subunit of the rapid rectifier potassium channel of HERG and MiRP1 genes resulting in slowing of cardiac potassium channels. It is characterized by prolonged QT
Keywords:
syndrome type;
congenital long;
long syndrome;
case misdiagnosed;
misdiagnosed arrhythmia;
type case
Journal Title: Journal of the American College of Cardiology
Year Published: 2019
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Journal Title: Journal of the American College of Cardiology
Year Published: 2019
Link to full text (if available)
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recommendations!