CONGENITAL LONG QT SYNDROME TYPE 2: THE CASE OF A MISDIAGNOSED ARRHYTHMIA AND A NEAR FALL FROM DEATH
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DOI: 10.1016/s0735-1097(19)33535-1
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… read more here.
Keywords: syndrome type; congenital long; long syndrome; case misdiagnosed ... See more keywords