RecruitingNCT02432079
Molecular Genetics of Heterotaxy and Related Congenital Heart Defects
Sponsor
Indiana University
Enrollment
2,000 participants
Start Date
Jul 1, 2009
Study Type
OBSERVATIONAL
Conditions
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
Inclusion Criteria2
- Subjects with heterotaxy and related congenital heart defects
- Family members of subjects with heterotaxy and related congenital heart defects
Exclusion Criteria2
- Subjects without heterotaxy and related congenital heart defects
- Family members of subjects without heterotaxy and related congenital heart defects
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Locations(1)
View Full Details on ClinicalTrials.gov
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NCT02432079
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