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Recruiting NCT02432079

Molecular Genetics of Heterotaxy and Related Congenital Heart Defects

Conditions: Heterotaxy Syndrome, Congenital Heart Defects

Sex: All
Healthy volunteers: No
Enrollment: 2000
Sponsor: Indiana University

Location: Indiana University School of Medicine Indianapolis Indiana

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 Criteria

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

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT02432079). StuddyBuddy aggregates publicly available trial information.