Molecular Genetics of Heterotaxy and Related Congenital Heart Defects

Conditions

• Congenital Heart Defects
• Heterotaxy Syndrome

Eligibility Criteria

Sex

ALL

Age

N/A - N/A

Healthy Volunteers

Not accepted

Study Details

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.

Key Dates

Start date

Jul 31, 2009

Status verified

Jun 2025

Primary completion

Dec 31, 2030

Completion

Dec 31, 2030

Study Design

Enrollment

2,000 participants (estimated)

Arms

• Arm: Heterotaxy and congenital heart defects
  Patients and family members with heterotaxy and related congenital heart defects

Primary Outcome Measure

Clarify Molecular Genetics of Heterotaxy and Related Congenital Heart Defects [ Time Frame: 8 years ]

Central Contacts

• Lindsey R. Helvaty, BA, BS
  317-278-3020
  [email protected]
• Stephanie M. Ware, MD, PhD
  317-278-2807
  [email protected]

Locations (1)

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