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Arrhythmogenic right ventricular cardiomyopathy masquerading as peripartum cardiomyopathy. [PDF]
HeartRhythm Case RepEzzeddine FM, Davis NE, Pereira NL.
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Early Recognition and Management of Arrhythmogenic Right Ventricular Cardiomyopathy in a Young Athlete: A Case Report Highlighting the Role of Multimodal Diagnosis and Preventive Implantable Cardioverter Defibrillator (ICD) Therapy. [PDF]
CureusMcClellan B +3 more
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Correction to: An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis. [PDF]
Eur Heart Jeuropepmc +1 more source
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Arrhythmogenic Right Ventricular Cardiomyopathy
New England Journal of Medicine, 2017Abstract Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heredo-familial heart muscle disease characterized by progressive myocardial atrophy with fibrofatty replacement. It is a rare disease with an estimated prevalence of 1:2000 to 1:5000.
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Arrhythmogenic Right Ventricular Cardiomyopathy
Heart Failure Clinics, 2010Arrhythmogenic right ventricular cardiomyopathy (ARVC) originally emerged as a pathologic diagnosis based on distinctive autopsy findings in cases of premature sudden death. Subsequently these characteristic pathologic features were associated with ventricular tachycardia of right ventricular origin and syncope.
Patrick T, Ellinor +2 more
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Arrhythmogenic Right Ventricular Cardiomyopathy
Pacing and Clinical Electrophysiology, 2009Arrhythmogenic right ventricular cardiomyopathy (ARVC) has evolved from postmortem pathology at to a diagnosable clinical condition, and holds promise for definitive genetic diagnosis. Its prevalence is between 1/1,000 and 1/5,000, with 10% of deaths occurring before age 19 and 50% before age 35.
BASSO, CRISTINA +4 more
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