Literature DB >> 6461310

Sudden death and partial absence of the right ventricular myocardium: a report of three cases and a review of the literature.

R Virmani, M Robinowitz, M A Clark, H A McAllister.   

Abstract

Three patients with congenital partial absence of the right ventricular myocardium were studied. These cases are unique in that all three patients died suddenly and none had clinical evidence of cardiovascular disease. Two of the three patients were active in sports, and both died suddenly while playing basketball. At the time of autopsy, the only significant abnormality was cardiomegaly, with right atrial and ventricular dilation and partial absence of the right ventricular myocardium.

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Year:  1982        PMID: 6461310

Source DB:  PubMed          Journal:  Arch Pathol Lab Med        ISSN: 0003-9985            Impact factor:   5.534


  3 in total

Review 1.  The arrhythmogenic right ventricle. Dysplasia versus cardiomyopathy.

Authors:  G Fontaine; F Fontaliran; F R Andrade; E Velasquez; J Tonet; X Jouven; Y Fujioka; R Frank
Journal:  Heart Vessels       Date:  1995       Impact factor: 2.037

2.  Arrhythmogenic right ventricular dysplasia.

Authors:  G Fòntaine
Journal:  Br Heart J       Date:  1993-09

3.  No detection of enteroviral genome in the myocardium of patients with arrhythmogenic right ventricular cardiomyopathy.

Authors:  F Calabrese; A Angelini; G Thiene; C Basso; A Nava; M Valente
Journal:  J Clin Pathol       Date:  2000-05       Impact factor: 3.411

  3 in total

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