Congenital Heart Disease GEnetic NEtwork Study (CHD GENES)

Launched by CHILDREN'S HOSPITAL MEDICAL CENTER, CINCINNATI · Sep 3, 2010

Keywords

ClinConnect Summary

The Congenital Heart Disease GEnetic NEtwork Study (CHD GENES) is a research study focused on understanding the genetic causes of congenital heart defects (CHD), which are heart problems present at birth and affect about 8 out of every 1,000 babies. This study aims to collect DNA and health information from participants to better understand how genes may influence the severity and outcomes of these heart defects. By doing this, researchers hope to find common genetic factors that contribute to CHD and how they may impact patients' health.

Anyone interested in joining the study needs to provide a signed consent form. However, some individuals won't qualify, such as those with specific minor heart conditions like isolated patent foramen ovale or certain types of heart issues related to premature birth. Participants will have their genetic material collected and will be asked questions about their health, which will help researchers gather detailed information to make important discoveries about congenital heart disease. This is an exciting opportunity to contribute to research that could lead to better treatments and outcomes for future patients.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • • Signed consent form
• Exclusion Criteria:
• • Isolated patent foramen ovale
• • Isolated prematurity-associated patent ductus arteriosus