Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Scientists hunt for heart defect genes in families

NCT ID NCT01192048

First seen Apr 13, 2026 · Last updated May 22, 2026 · Updated 7 times

Summary

This study aims to find the genetic causes of congenital heart disease, the most common birth defect. Researchers will use whole genome sequencing to analyze DNA from up to 5,000 people with the condition and their relatives. No treatment is offered; the goal is to better understand why these heart defects occur.

Disclaimer Read more

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for CONGENITAL HEART DISEASE are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Nationwide Children's Hospital

    RECRUITING

    Columbus, Ohio, 43205, United States

    Contact

Conditions

Explore the condition pages connected to this study.