University of Massachusetts Medical School Faculty Publications

Title

Post-mortem genetic testing in a family with long-QT syndrome and hypertrophic cardiomyopathy

UMMS Affiliation

Department of Pediatrics, Division of Cardiology

Publication Date

3-1-2014

Document Type

Article

Subjects

Adolescent; Autopsy; Cardiomyopathy, Hypertrophic, Familial; Cardiovascular Agents; Child; Child, Preschool; Death, Sudden, Cardiac; Ether-A-Go-Go Potassium Channels; Fatal Outcome; Female; Genetic Predisposition to Disease; *Genetic Testing; Humans; Long QT Syndrome; Male; *Mutation, Missense; Pedigree; Predictive Value of Tests; Troponin T

Disciplines

Cardiology | Cardiovascular Diseases | Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Pathology | Pediatrics

Abstract

Pediatric sudden unexplained deaths are rare and tragic events that should be evaluated with all the tools available to the medical community. The current state of genetic testing is an excellent resource that improves our ability to diagnose cardiovascular disorders that can lead to sudden cardiac arrest. Post-mortem genetic testing is not typically a covered benefit of health insurance and may not be offered to families in the setting of a negative autopsy. This unusual case includes two separate cardiovascular disorders that highlight the use of genetic testing and its role in diagnosis, screening, and risk stratification. The insurance company's decision to cover post-mortem testing demonstrated both compassion as well as an understanding of the long-term cost effectiveness.

Rights and Permissions

Citation: Cardiovasc Pathol. 2014 Mar-Apr;23(2):107-9. doi: 10.1016/j.carpath.2013.11.003. Link to article on publisher's site.

Related Resources

Link to Article in PubMed

Keywords

Familial cardiomyopathy screening, Hypertrophic cardiomyopathy, Long QT syndrome, Post-mortem genetic testing, Sudden cardiac arrest

Journal/Book/Conference Title

Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology

PubMed ID

24322056