A case series of desmoplakin cardiomyopathy: a mimic of viral myocarditis.
Kaveh Rezaei BookaniIva MingaJoshua WodskowJordan HarrisRobert GordonNitasha SarswatAmit PursnaniPublished in: European heart journal. Case reports (2022)
Mutations in the DSP gene are associated with left dominant arrhythmogenic cardiomyopathy, which is a variant of ARVC. Beside left ventricular systolic dysfunction and ventricular tachyarrhythmias, carriers of these mutations may present with episodes of chest pain associated with elevated cardiac enzymes and cardiac imaging findings indistinguishable from other forms of acute myocarditis including viral myocarditis. Currently, there are no guidelines for diagnosis and treatment of this entity.
Keyphrases
- left ventricular
- heart failure
- hypertrophic cardiomyopathy
- sars cov
- cardiac resynchronization therapy
- acute myocardial infarction
- mitral valve
- aortic stenosis
- left atrial
- liver failure
- high resolution
- oxidative stress
- genome wide
- drug induced
- gene expression
- atrial fibrillation
- aortic dissection
- fluorescence imaging
- transcatheter aortic valve replacement
- mass spectrometry
- coronary artery disease
- genome wide identification