Molecular genetics of familial heart disease

Completed

• Conditions: congenital heart defect; Congenital heart disease; 10010394; 10007510

• Registration Number: NL-OMON37798
• Lead Sponsor: Academisch Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 300

Inclusion Criteria

Individuals from families with two or more affected persons with congenital heart disease and/or (thoracic) aortic aneurysm are included. Affected family members as well as unaffected family members are included.

Exclusion Criteria

None

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Genetic defects underlying CHD and aortic aneurysms.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Not applicable</p><br>