Genetic mapping for multiple birth defects or intellectual disability
Treatments studied
Part of Genetic & congenital clinical trials.
This study uses a new genetic technique to find hidden causes in people with multiple birth defects or intellectual disability who had standard genetic tests come back normal. It might help identify a genetic reason when other tests did not.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have at least two birth defects, with or without intellectual disability.
- You weigh more than 11 pounds (5 kg).
- You already had whole-genome sequencing that did not find a clear genetic cause.
- You are covered by health insurance (social security).
- You can understand the study and agree to participate (or a parent/guardian can).
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 uses advanced genetic tests to find the cause of severe intellectual disability or related developmental disorders when standard tests found nothing. If you or your child qualify, the study may provide a clearer diagnosis and help guide care.
This study uses trio genome sequencing (comparing DNA from you and both of your parents) to find genetic causes for psychiatric disorders that start early, are hard to treat, or have an unusual pattern. It may help if you or your child have a mental health condition without intellectual disability or birth defects.
This trial uses genetic testing to better understand the cause of a newborn’s birth defect and to help doctors choose more personalized treatment. It may help families get clearer answers and more targeted care.
This study uses genome (DNA) sequencing to look for the genetic cause of rare disorders, especially when the cause is unknown. It may help some families better understand what is driving the condition, using genetic information from the affected person and often their parents.
This study helps identify genetic causes of birth defects that weren't found by standard tests. Researchers use advanced genetic mapping to look for structural changes in DNA that might explain your baby's condition.
This study is looking for people with rare, unexplained conditions that cause early intellectual disability and low muscle tone. Researchers want to study your cells and blood to try to find new genetic causes that standard DNA tests missed.
Hear when a new Congenital Malformations trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.