Arrhythmogenic Right Ventricular Cardiomyopathy Caused by a Novel Frameshift Mutation

dc.contributor.authorRefaat, Marwan M.
dc.contributor.authorTang, Paul Ling Fung
dc.contributor.authorHarfouch, Nassier
dc.contributor.authorWojciak, Julianne
dc.contributor.authorKwok, Puiyan Yan
dc.contributor.authorScheinman, Melvin M.
dc.contributor.departmentInternal Medicine
dc.contributor.departmentBiochemistry and Molecular Genetics
dc.contributor.departmentDivision of Cardiology
dc.contributor.departmentCardiac Electrophysiology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:48:45Z
dc.date.available2025-01-24T11:48:45Z
dc.date.issued2016
dc.description.abstractArrhythmogenic right ventricular cardiomyopathy is a rare cardiomyopathy that might be asymptomatic or symptomatic, causing palpations or syncope, and might lead to sudden cardiac death. It is recommended that physical exertion be reduced. It is also recommended that those with syncope and ventricular tachycardia/ventricular fibrillation have an implantable cardioverter-defibrillator placed. beta-Blockers, antiarrhythmic drugs, and radiofrequency ablation should be used to control the ventricular arrhythmia burden in arrhythmogenic right ventricular cardiomyopathy.
dc.identifier.doihttps://doi.org/10.1016/j.ccep.2015.10.033
dc.identifier.eid2-s2.0-84960077486
dc.identifier.pmid26920198
dc.identifier.urihttp://hdl.handle.net/10938/30840
dc.language.isoen
dc.publisherW.B. Saunders
dc.relation.ispartofCardiac Electrophysiology Clinics
dc.sourceMedline
dc.subjectArrhythmogenic right ventricular dysplasia/diagnosis/diagnostic
dc.subjectImaging/genetics/physiopathology
dc.subjectElectrocardiography
dc.subjectFrameshift mutation/genetics
dc.subjectHumans
dc.subjectMale
dc.subjectMiddle aged
dc.subjectPlakophilins/genetics
dc.subjectSyncope
dc.subjectArrhythmogenic right ventricular cardiomyopathy
dc.subjectPkp2 gene
dc.subjectPalpitations
dc.titleArrhythmogenic Right Ventricular Cardiomyopathy Caused by a Novel Frameshift Mutation
dc.typeReview

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