Utility of genetics for risk stratification in pediatric hypertrophic cardiomyopathy

Children with hypertrophic cardiomyopathy (HCM) experience sudden cardiac death (SCD) and other life‐threatening events. We assessed if affected gene and variant burden predict outcomes. Patients

Saved in:
Bibliographic Details
Published in:Clinical genetics 2018-02, Vol.93 (2), p.310-319
Main Authors: Mathew, J., Zahavich, L., Lafreniere‐Roula, M., Wilson, J., George, K., Benson, L., Bowdin, S., Mital, S.
Format: Article
Language:English
Subjects:
Cardiomyopathy
Children
Defibrillators
Electrocardiography
genetics
Heart diseases
hypertrophic cardiomyopathy
Insertion
myectomy
myosin
Pediatrics
sudden death
Transplantation
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Children with hypertrophic cardiomyopathy (HCM) experience sudden cardiac death (SCD) and other life‐threatening events. We assessed if affected gene and variant burden predict outcomes. Patients
ISSN:0009-9163
1399-0004
DOI:10.1111/cge.13157