Subclinical Cardiomyopathy and Long QT Syndrome: An Echocardiographic Observation

Author:

Haugaa Kristina H.1,Johnson Jonathan N.2,Bos J. Martijn3,Phillips Brandon Lane2,Eidem Benjamin W.2,Ackerman Michael J.

Affiliation:

1. Department of Internal Medicine/Division of Cardiovascular Diseases; Mayo Clinic; Rochester; Minn; USA

2. Department of Pediatrics/Division of Pediatric Cardiology; Mayo Clinic; Rochester; Minn; USA

3. Department of Molecular Pharmacology & Experimental Therapeutics; Mayo Clinic; Rochester; Minn; USA

Publisher

Computers, Materials and Continua (Tech Science Press)

Subject

Cardiology and Cardiovascular Medicine,Radiology Nuclear Medicine and imaging,General Medicine,Surgery,Pediatrics, Perinatology, and Child Health

Reference31 articles.

1. Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death;Jervell;Am Heart J.,1957

2. Rare cardiac arrythmias of the pediatric age. II. Syncopal attacks due to paroxysmal ventricular fibrillation (presentation of 1st case in Italian pediatric literature);Romano;Clin Pediatr (Bologna).,1963

3. A new familial cardiac syndrome in children;Ward;J Ir Med Assoc.,1964

4. Prevalence of the congenital long-QT syndrome;Schwartz;Circulation.,2009

5. Mutation of an A-kinase-anchoring protein causes long-QT syndrome;Chen;Proc Natl Acad Sci U S A.,2007

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