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