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Molecular Genetics Of Heterotaxy And Related Congenital Heart Defects

Investigating the Genetics of Heterotaxy and Congenital Heart Defects

Recruiting
100 years and younger
All
Phase N/A
  • Simplified description (AI rewritten)
  • Technical description (Original)

This study investigates the genetics behind heterotaxy and related congenital heart defects. Heterotaxy is a condition where the internal organs are abnormally arranged within the chest and abdomen. The purpose of the study is to gather information from affected individuals and their families to better understand the genetic causes of these conditions.

Participants will provide specimens and data for research. This involves collecting samples and information that will help researchers study the molecular genetics of heterotaxy and related heart defects.

  • Who can participate: Individuals with heterotaxy and related congenital heart defects, along with their family members, are eligible to participate. Individuals without heterotaxy and related congenital heart defects, and their family members, are not eligible to participate.
  • Study details: Participants will provide specimens and data.
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Study details
    heterotaxy
    congenital heart defect
    chd
    heart defect
    congenital

TX6875

19 February 2024

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