Home › Congenital Heart Defects › NCT02432079

Molecular Genetics of Heterotaxy and Related Congenital Heart Defects

Who can join

All ages · All sexes

Inclusion Criteria:

* Subjects with heterotaxy and related congenital heart defects
* Family members of subjects with heterotaxy and related congenital heart defects

Exclusion Criteria:

* Subjects without heterotaxy and related congenital heart defects
* Family members of subjects without heterotaxy and related congenital heart defects

About the study

The goal of this study is to obtain specimens and data from individuals and their families with heterotaxy and related congenital heart defects in order to clarify the molecular genetics of this disorder. The knowledge gained from the analysis of this information will provide the basis for future genetic counseling as well as contribute to knowledge about the biology of normal and abnormal development of left-right anatomic asymmetry.

Sponsor: Indiana University · Participants: 2,000 · Started: 2009-07

Contact the study team

• Sarah K. Murphy, MPH · Phone: 317-278-3026
• Stephanie M. Ware, MD, PhD · Phone: 317-278-2807

Official record on ClinicalTrials.gov — NCT02432079

Locations in the U.S.

Conditions

• Congenital Heart Defects
• Birth Defects
• Cardiovascular Disease
• Heart Diseases

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.