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Genetics of Cardiovascular and Neuromuscular Disease

Arrhythmia Clinical Trial

Official title:
Genetic Studies of Patients and Their Families With Inherited Cardiovascular and Neuromuscular Diseases.

Clinical Trial Summary

We are studying the genetics of human cardiovascular and neuromuscular disease. There are many different genetic regions that have been associated with the development of cardiomyopathy. An equal number of genetic regions have been associated with muscular dystrophy and there is overlap because some of the identical genes, when mutated, produce both cardiomyopathy and muscular dystrophy. We are working to identify genes and gene mutations associated with cardiomyopathy, arrhythmias and muscular dystrophy. We propose to screen these samples for mutations in genes known to be involved in these disorders.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00138931
Study type Observational
Source University of Chicago
Contact Lisa Dellefave, MS
Phone 773-702-4310
Email Ldellefa@medicine.bsd.uchicago.edu
Status Recruiting
Phase
Start date September 1996
Completion date January 2025
View Details
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