Literature DB >> 3581542

Arrhythmogenic right ventricular dysplasia presenting with ventricular tachycardia in a father and son.

C B-Lundqvist, S Eneström, N Edvardsson, S B Olsson.   

Abstract

A father and his son presented with ventricular tachycardia of left bundle-branch block configuration, two years apart. The patients had no clinical signs of right or left ventricular dysfunction. The diagnosis of arrhythmogenic right ventricular dysplasia was based on right ventricular angiographic and radionuclide findings. Microscopic sections obtained at surgery for the ventricular tachycardia in the father revealed abnormal infiltration of fat and focal fibrosis in the right ventricular myocardium, confirming the diagnosis. The importance of thorough evaluation of right and left ventricular function and structure in patients with ventricular tachycardia of right ventricular origin is emphasized. Currently available diagnostic techniques and management are presented.

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Year:  1987        PMID: 3581542     DOI: 10.1002/clc.4960100415

Source DB:  PubMed          Journal:  Clin Cardiol        ISSN: 0160-9289            Impact factor:   2.882


  3 in total

1.  A novel variant in plakophilin-2 gene detected in a family with arrhythmogenic right ventricular cardiomyopathy.

Authors:  Bozena Ostrowska Dahlgren; Marie Allen; Anne-Cristine Lindström; Mia Bjerke; Carina Blomström-Lundqvist
Journal:  J Interv Card Electrophysiol       Date:  2011-12-15       Impact factor: 1.900

2.  A long term follow up of 15 patients with arrhythmogenic right ventricular dysplasia.

Authors:  C Blomström-Lundqvist; K G Sabel; S B Olsson
Journal:  Br Heart J       Date:  1987-11

3.  Dysplastic conditions of the right ventricular myocardium: Uhl's anomaly vs arrhythmogenic right ventricular dysplasia.

Authors:  L M Gerlis; S C Schmidt-Ott; S Y Ho; R H Anderson
Journal:  Br Heart J       Date:  1993-02
  3 in total

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