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Patients with likely pathogenic/pathogenic desmoplakin (dsp) variants are poorly characterized Data describing arrhythmic outcomes of patients harboring a likely pathogenic/pathogenic (lp/p) desmoplakin (dsp) variant and fulfilling a definite diagnosis of arrhythmogenic cardiomyopathy. Some of them meet diagnostic criteria for arrhythmogenic right ventricular.

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Aims desmoplakin (dsp) cardiomyopathy is an increasingly recognized form of arrhythmogenic cardiomyopathy Arrhythmogenic cardiomyopathy (acm) is a heterogeneous genetic disease characterized by fibrofatty infiltration of the myocardium and the development of potentially. Dsp cardiomyopathy is a distinct form of arrhythmogenic cardiomyopathy characterized by episodic myocardial injury, left ventricular fibrosis that precedes systolic.

Desmoplakin (dsp) genetic variants have been reported in arrhythmogenic cardiomyopathy with particular regard to predominant left ventricular (lv) involvement.

Desmoplakin cardiomyopathy affects both ventricles and carries high risk for ventricular arrhythmia and heart failure Myocardial injury is prospectively associated. However the genetic architecture and.