Pediatric Cardiomyopathy Mutation Analysis

Overview

The purpose of the study is to identify genes related to pediatric cardiomyopathy, a disease that causes poor function of the heart muscle.

Description

The purpose of this study is to identify genes related to pediatric cardiomyopathy.

Eligibility

You may be eligible for this study if you meet the following criteria:

  • Conditions: cardiomyopathy,genetic,dilated,restrictive,hypertrophic,arvc,genetics,cardiomyopathies,pediatric,familial,dcm,rcm,hcm,left ventricle,lvnc,heart muscle disease,heart disease,heart,cardiology,pediatric,kid,kids,child,children,adolescent,youth,riley,cardiomyopathy,heart muscle disease,heart disease,heart,cardiology,pediatric,kid,kids,child,children,adolescent,youth,riley
  • Age: - 100 Years
  • Gender: Male or Female

Inclusion Criteria
Patients with cardiomyopathy
Family members of subjects with cardiomyopathy
Exclusion Criteria
Patients without cardiomyopathy
Family members of subjects without cardiomyopathy

Additional Information:

Updated on 20 Nov 2022 . Study ID: TX6881

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What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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