Studying unknown movement disorders in children in Vietnam
Part of Brain & nervous system, Genetic & congenital clinical trials.
This trial is for children in Vietnam who have a movement disorder with an unknown cause. Researchers want to learn more by doing genetic testing, which might help find better treatments or answers for families.
Summary written for real people, not researchers, by Clin2.
Who can take part
- Your child is under 18 years old.
- Your child has a movement disorder diagnosed by at least two pediatric neurologists.
- The cause of the movement disorder is not yet known after standard tests.
- Your child is being treated or evaluated at one of the two hospitals in Ho Chi Minh City.
- You and your child agree to sign a consent form and provide samples for genetic testing.
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 looks at children with epilepsy and movement disorders to better understand the genes involved. It aims to help doctors recognize and treat these conditions more effectively.
This study is creating a registry to track the health of people who have specific genetic changes that cause epilepsy and uncontrolled movements (dyskinesia). It may help researchers better understand these conditions and how they change over time.
This study looks for genetic reasons that may contribute to cerebral palsy. It may help families understand potential causes, especially when a specific genetic change is found.
This study is for children or adults with neurodevelopmental conditions and unusual physical features, where standard genetic tests haven't found a cause. Researchers will use RNA and DNA sequencing to look for hidden genetic explanations, which could guide better care.
This study looks at DNA (genetic material) in people with movement disorders or dementia, and in some family members or healthy volunteers. The goal is to better understand why these conditions happen and how genes may contribute.
This study looks for biological “markers” (measurable signs in the body) in people with inherited movement disorders, and in some related family members or healthy volunteers. It may help researchers better understand these conditions, especially for future diagnosis and care.
Hear when a new Movement Disorders in Children trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.