A rare cause of 2:1 AV block: Long QT syndrome

Journal of Cardiovascular Electrophysiology

Volumn 19, Issue 9, 2008, Pages 990-

  Patel, Chinmay ^a   Narayanaswamy, Srinivasa ^a   Medina Ravell, Victor A ^b   Yan, Gan Xin ^a,c  

^a Main Line Health Heart Center   (United States)

^b Centro Medico Dr Rafael Guerra Mendez   (Venezuela)

^c THOMAS JEFFERSON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ARTIFICIAL HEART PACEMAKER; ATRIOVENTRICULAR BLOCK; CASE REPORT; DEFIBRILLATOR; FEMALE; HEART ATRIOVENTRICULAR NODE; HUMAN; P WAVE; PRESCHOOL CHILD; PRIORITY JOURNAL; QT INTERVAL; QT PROLONGATION; SINUS BRADYCARDIA; T WAVE; TELEMETRY; TORSADE DES POINTES;

ATRIOVENTRICULAR BLOCK; CHILD; DEFIBRILLATORS, IMPLANTABLE; FEMALE; HUMANS; LONG QT SYNDROME; RARE DISEASES;

EID: 50449108729     PISSN: 10453873     EISSN: 15408167     Source Type: Journal    
DOI: 10.1111/j.1540-8167.2008.01113.x     Document Type: Article

References (1)

1. Lupoglazoff JM, Denjoy I, Villain E, Fressart V, Legall-Petit I, Bozio A, Berthet M, Benammar N, Hainque B, Guicheney P : Neonatal forms of congenital long QT syndrome. Arch Mal Coeur Vaiss 2004 97 : 479 483.