Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

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DiscussionARVC is a genetic diseaseMutations affect genes coding desmosomal proteinsPrimary function is forming intercellular junction andcell adhesion; disruption leads to cell death and tissueremodelingCharacterized by structural and functional abnormalitiesiof right ventricle, fibro-fatty fatty and scar tissue replacementresults in ventricular tachycardia, RV failure or suddencardiac death20% of SCD among young individuals
Mechanical Stress on impaired desmosomalproteins Myocyte detachment and death
Page 1 and 2: Arrhythmogenic Right VentricularDys
Page 3 and 4: Learning ObjectivesCharacteristics
Page 5: Case PresentationChief Complaint: I
Page 9 and 10: Physical ExamVitals: Temp 96.7, BP
Page 11 and 12: Wide Complex Regular Tachycardia+ Q
Page 13 and 14: LabsTroponins: 0.120.21.3 2.20 1.8
Page 15 and 16: CCU CourseContinued on amiodarone g
Page 17 and 18: Cardiac MRIRevealed right ventricle
Page 19 and 20: Cardiac MRIShort axis viewdemonstra
Page 21: Final OutcomeEvaluated by EP, s/p I
Page 25 and 26: Coronary Syndrome XPatients have an
Page 27 and 28: History/EpidemiologyNewly recognize
Page 29 and 30: Diagnosis: Task Force CriteriaI. Gl
Page 31 and 32: Epsilon waves,which h arereproducib
Page 33 and 34: V. ArrhythmiasMinor:- LBBB type ven
Page 35 and 36: Evaluation of Risk Factors SCD in A
Page 37 and 38: Discussion:- ARVD typically present
Page 39 and 40: Genetic TestingFamily ScreeningFami
Page 41 and 42: ReferencesMcNally E, MacLeod H, Del

Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

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