Pediatric Cardiomyopathy Mutation Analysis

Investigation of Genetic Factors in Pediatric Cardiomyopathy

Recruiting
100 years or below
All
Phase N/A
1 Location

Brief description of study.

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

Detailed description of study

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

Participants may be compensated for their participation.

Eligibility of study

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

  • Conditions: cardiomyopathy,heart muscle disease,heart disease,heart,cardiology,pediatric,kid,kids,child,children,adolescent,youth,riley
  • Age: 100 years or below
  • Gender: All

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

Updated on 19 Feb 2024. Study ID: 1403919054

This study investigates the genetic factors associated with pediatric cardiomyopathy, a condition that affects the heart muscle's ability to function properly. By understanding the genetic components, researchers hope to gain insights into the causes and potential ways to address this condition.

Participants in the study will undergo genetic testing to identify specific genes related to cardiomyopathy. Genetic testing involves analyzing DNA to find changes or mutations that could be linked to the disease.

  • Who can participate: Children diagnosed with cardiomyopathy and their family members are eligible to participate. Individuals without cardiomyopathy or family members of those without the condition are not eligible.
  • Study details: Participants will be involved in genetic testing, which includes a DNA analysis to identify potential genetic mutations associated with cardiomyopathy.

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