Managing Secondary Genomic Findings Associated With Arrhythmogenic Right Ventricular Cardiomyopathy: Case Studies and Proposal for Clinical Surveillance

Circ Genom Precis Med. 2018 Jul;11(7):e002237. doi: 10.1161/CIRCGEN.118.002237.

Authors

Affiliations

¹ Geisinger, Danville, PA (C.M.H., M.S., A.C.S., M.E.M., M.F.M., B.K.F.). chaggerty3@gatech.edu.
² Geisinger, Danville, PA (C.M.H., M.S., A.C.S., M.E.M., M.F.M., B.K.F.).
³ Johns Hopkins Medical Center, Baltimore, MD (B.M., C.T., D.P.J., H.T., H.C., C.A.J.).
⁴ Medical University of South Carolina, Charleston, SC (D.P.J.).
⁵ Yale School of Medicine, New Haven, CT (M.F.M.).

PMID: 29997227
DOI: 10.1161/CIRCGEN.118.002237

No abstract available

Keywords: arrhythmogenic right ventricular dysplasia; exome; genetics, medical; genomics; penetrance.

Publication types

Case Reports
Research Support, Non-U.S. Gov't

MeSH terms

Adult
Aged
Arrhythmogenic Right Ventricular Dysplasia / diagnosis*
Arrhythmogenic Right Ventricular Dysplasia / genetics*
Arrhythmogenic Right Ventricular Dysplasia / physiopathology*
Child
Female
Genomics*
Humans
Male