Genetic testing for children with heart defects
Part of Genetic & congenital, Heart & circulation clinical trials.
This study looks at chromosomal changes in children born with heart problems. It aims to find genetic links that could help explain why some heart defects happen.
Summary written for real people, not researchers, by Clin2.
Who can take part
- Your child has a heart condition they were born with.
- Age between 1 month and 18 years.
- Your child is a patient at Assiut University Children's Hospital or Elmabara Insurance Hospital.
- You as a parent or guardian agree to participate and sign a consent form.
- Your child is not critically ill and can safely have a blood draw.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
Similar studies
Other trials that look related to this one.
This study is building a network of hospitals across China to help children with congenital heart disease. If your child was born with a heart problem and is under 18, they may be able to join and help improve care for kids like them.
This study tests a new way to find genetic causes of congenital heart disease (a heart problem found before birth) using samples from amniocentesis or chorionic villus sampling. It may help parents get a clearer diagnosis and plan for their baby's care.
This study tests the chromosomes of children with birth defects or developmental delays to find genetic causes. It may help families understand why their child has these conditions.
This study looks at how genes may contribute to congenital heart disease. It may help researchers better understand causes and risk in families like yours.
This trial studies children with inherited (genetic) heart conditions that started before age 16. It may help improve how doctors identify the genetic cause and understand which families are affected.
This study looks at the genetic material in the fluid around the baby (amniotic fluid) and in the placenta to better understand complex heart defects in unborn babies. The goal is to find new clues that could help doctors care for these babies before and after birth.
Hear when a new Chromosomal Abnormalities trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.