Cardiology

• R127 Long QT syndrome (LQTS)
  Genetic testing for Long QT syndrome (LQTS) (R127)
• R128 Brugada syndrome and cardiac sodium channel disease
  Genetic testing for Brugada syndrome (R128)
• R129 Catecholaminergic polymorphic VT (CPVT)
  Genetic testing for Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) (R129)
• R130 Short QT syndrome (SQTS)
  Genetic testing for Short QT syndrome (SQTS) (R130)
• R131 Hypertrophic cardiomyopathy (HCM)
  Genetic testing for hypertrophic cardiomyopathy (HCM) (R131)
  
• R132 Dilated and arrhythmogenic cardiomyopathy (DCM)
  Genetic testing for dilated and arrhythmogenic cardiomyopathy (DCM) (R132)
• R133 Arrhythmogenic cardiomyopathy
  Genetic testing for arrhythmogenic cardiomyopathy (R133)
• R134 Familial hypercholesterolemia
  Genetic testing for familial hypercholesterolaemia (R134)
• R135 Paediatric or syndromic cardiomyopathy
  Genetic testing for paediatric cardiomyopathy (PaedCM) (R135)
• R138 Molecular autopsy following sudden unexplained death
  Genetic testing for cardiac arrhythmia of unknown type (Molecular Autopsy) (R138)
• R328 Progressive cardiac conduction disease
  Genetic testing for progressive cardiac conduction disease (PCCD)(R328)

Testing for previously identified familial variants, as clinically appropriate, is available.

Research

The laboratory is closely involved with the Watkins Research Group: Inherited Heart muscle Disease Group.

Further information on the cardiac genetics research undertaken by this group is available on the Radcliffe Department of Medicine Medical Sciences Division website.