Short QT Syndrome (SQTS)

  • Vincent E. Friedewald
Chapter

Abstract

NS

Keywords

Quinidine Hypercalcemia Disopyramide 

Guidelines

  1. HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes Google Scholar
  2. Heart Rhythm. 2013;10:1932–63.Google Scholar

Patient Information

  1. Genetics Home ReferenceGoogle Scholar

Professional Information

  1. Circulation Arrhythmia Electrophysiol. 2010;3:401–8. http://circep.ahajournals.org/content/3/4/401.full.

Review

  1. Ann Noninvasive Electrocardiol. 2005;10:371–7. http://www.ncbi.nlm.nih.gov/pubmed/16029390.

Review

Review

  1. Acta Cardiol. 2008;63:553–5. http://www.ncbi.nlm.nih.gov/pubmed/19013996.

Review: Genetics of Sudden Cardiac Death

  1. Circulation Research. 2015;116:1919–36. http://circres.ahajournals.org/content/116/12/1919.full.

Children: Long-Term Follow-Up

Clinical/Medical Genetics

  1. Curr Opin Cardiol. 2008;23:192–8. http://www.ncbi.nlm.nih.gov/pubmed/18382206.

Early Repolarization: Prevalence

Echocardiography

Mutation: KCNJ2 Gene

  1. Proc Natl Acad Sci USA. 2013;110:4291–6. http://www.pnas.org/content/110/11/4291.full.

Mutation: SQTS6 Gene

Natural History

Ventricular Arrhythmias in Channelopathies: Management

  1. Circulation Arrhythmia Electrophysiol. 2015;8:221–31. http://circep.ahajournals.org/content/8/1/221.extract?etoc.

Copyright information

© Springer-Verlag London 2016

Authors and Affiliations

  • Vincent E. Friedewald
    • 1
  1. 1.Division of CardiologyUT Health Science Center at Houston Division of CardiologyHoustonUSA

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