Observational Study: Mapping Disease Pathways for Biliary Atresia
This observational study aims to understand the genetic causes of Biliary Atresia (BA), a serious liver condition in babies that often requires a liver transplant. Researchers will look at the genetic makeup of people with BA to find out what pathways are involved in the disease. The study is trying to understand if there are genetic differences between the 'isolated' form of BA, thought to be caused by viruses, and the 'syndromic' form, which is linked to other birth defects. The goal is to identify the genomic pathways of BA. You may be able to join if you have Biliary Atresia and have received or are about to receive a liver transplant at one of the participating hospitals: Children's Hospital of Pittsburgh, Kings College Hospital, Children's Hospital of Birmingham, or Hospital Sírio-Libanês. The study is currently unclear on its recruitment status.
- Study design
- This is an observational study planning to include 1100 participants. It is not testing a specific treatment.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- The genomic pathways of BA will be measured for up to two years.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Mapping Disease Pathways for Biliary Atresia
At a glance
Conditions
Where it's being run
1 sites across 1 statesWho to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Genomic pathways of BAup to two years
Main project outcome will consist of pathways comprising multiple susceptibility genes involved in morphogenesis of the liver and other organs, which explain the complex phenotype of BA.