Molecular Genetics Of Heterotaxy And Related Congenital Heart Defects

Recruiting
100 years or below
All
Phase N/A
1 Location

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.

Participants may be compensated for their participation.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: heterotaxy,congenital heart defect,chd,heart defect,congenital
  • Age: 100 years or below
  • 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

Updated on 04 Aug 2024. Study ID: 1403871897

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