Molecular Genetics Of Heterotaxy And Related Congenital Heart Defects
S
Stephanie Ware, MD
Primary Investigator
Recruiting
100 years or below
All
Phase
N/A
3 Locations
Brief description of study
The purpose of this study is to obtain information from individuals and their families with heterotaxy and related congenital heart defects in order to elucidate the molecular genetics of this disorder.
Detailed description of 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.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: heterotaxy, congenital heart defect, Riley
-
Age: 100 years or below
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Gender: All
Inclusion Criteria
Patients with heterotaxy and related congenital heart defects
Family members of patients with heterotaxy and related congenital heart defects
Exclusion Criteria
Patients without heterotaxy and related congenital heart defects
Family members of patients without heterotaxy and related congenital heart defects
Additional Information:Patients with heterotaxy and related congenital heart defects
Family members of patients with heterotaxy and related congenital heart defects
Exclusion Criteria
Patients without heterotaxy and related congenital heart defects
Family members of patients without heterotaxy and related congenital heart defects
Participants may be compensated for their participation.
Updated on
23 Sep 2024.
Study ID: 1403871897, PEDS-IIR-WARE-HTX
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