Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a review and update
Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a review and update
About this item
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Author / Creator
Publisher
Berlin/Heidelberg: Springer-Verlag
Journal title
Language
English
Formats
Publication information
Publisher
Berlin/Heidelberg: Springer-Verlag
Subjects
More information
Scope and Contents
Contents
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a predominantly genetically determined and heritable form of cardiomyopathy that is characterized pathologically by the replacement of myocytes by adipose and fibrous tissue and leads to right ventricular failure, arrhythmias, and sudden cardiac death. The estimated prevalence of...
Alternative Titles
Full title
Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a review and update
Authors, Artists and Contributors
Author / Creator
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Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_863423080
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_863423080
Other Identifiers
ISSN
1861-0684
E-ISSN
1861-0692
DOI
10.1007/s00392-011-0295-2
