|

Molecular Genetics of Heterotaxy and Related Congenital Heart Defects

RECRUITINGSponsored by Indiana University
Actively Recruiting
SponsorIndiana University
Started2009-07
Est. completion2030-12
Eligibility
Healthy vol.Accepted
Locations1 site
View on ClinicalTrials.gov →

NCT02432079

Summary

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.

Eligibility

Healthy volunteers accepted
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

Conditions3

Congenital Heart DefectsHeart DiseaseHeterotaxy Syndrome

Locations1 site

Indiana University School of Medicine
Indianapolis, Indiana, 46202
Lindsey R Helvaty, BA, BS317-278-3020lhelvaty@iu.edu

Browse More Trials

Heart Disease trials

Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

This site does not provide medical advice. Always consult your doctor before considering enrollment in a clinical trial. Learn more on our About page.