Recurrent immunosuppressive-responsive myocarditis in a patient with desmoplakin cardiomyopathy: a case report
Author:
Affiliation:
1. Department of Cardiology, Royal Prince Alfred Hospital , 50 Missenden Road, Camperdown, New South Wales 2050 , Australia
2. Faculty of Medicine and Health, The University of Sydney , Science Road, Camperdown, New South Wales 2050 , Australia
Abstract
Publisher
Oxford University Press (OUP)
Link
https://academic.oup.com/ehjcr/advance-article-pdf/doi/10.1093/ehjcr/ytae129/56961447/ytae129.pdf
Reference10 articles.
1. Clinical characteristics and risk stratification of desmoplakin cardiomyopathy;Wang;Europace,2022
2. Desmoplakin cardiomyopathy, a fibrotic and inflammatory form of cardiomyopathy distinct from typical dilated or arrhythmogenic right ventricular cardiomyopathy;Smith;Circulation,2020
3. 2023 ESC guidelines for the management of cardiomyopathies: developed by the task force on the management of cardiomyopathies of the European Society of Cardiology (ESC);Arbelo;Eur Heart J,2023
4. Left-dominant arrhythmogenic cardiomyopathy: an under-recognized clinical entity;Sen-Chowdhry;J Am Coll Cardiol,2008
5. Defining the interactions between intermediate filaments and desmosomes;Smith;J Cell Biol,1998
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