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Diagnoses evaluated

Patients with the following documented diagnoses:

  • Atrial and ventricular ectopy

  • Tachycardia (both supraventricular and ventricular)

  • Pathologic bradycardia

  • Wolff-Parkinson-White Syndrome

  • Unexplained QTc prolongation

  • Inheritable channelopathies (Long QT Syndrome, Short QT Syndrome, Brugada Syndrome, Catecholaminergic Polymorphic Ventricular Tachycardia)

  • Arrhythmogenic Right Ventricular Cardiomyopathy

  • Risk stratification for sudden arrhythmogenic death in individuals with repaired tetralogy of Fallot, hypertrophic cardiomyopathy, and dilated cardiomyopathy

Patients with a family history of the following diagnoses:

  • Unexplained sudden death (including Sudden Infant Death Syndrome)

  • Inheritable channelopathies (Long QT Syndrome, Short QT Syndrome, Brugada Syndrome, Catecholaminergic Polymorphic Ventricular Tachycardia)

  • Arrhythmogenic Right Ventricular Cardiomyopathy