Scientists launch hunt for clues in rare childhood brain condition
NCT ID NCT07421219
Summary
This study aims to improve the understanding and future care for children with a rare, lifelong movement coordination disorder called non-progressive congenital ataxia. Researchers will observe 50 children across Europe, aged 5 to 8, to map their development, analyze brain scans, and look for genetic links. The goal is to create a detailed picture of the condition to help guide future research and support for affected families.
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Contacts and locations
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Study contacts
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Contact
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Contact
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Locations
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Aarhus University Hospital
Aarhus, Denmark
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IASO Children's Hospital
Athens, Greece
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KU Leuven
Leuven, Belgium
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Queen Silvia Children's Hospital at Sahlgrenska University Hospital
Gothenburg, 416 50, Sweden
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Toulouse University Hospital
Toulouse, France
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University Hospital Tübingen
Tübingen, Germany
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Vestfold Hospital Trust
Tønsberg, Norway
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Conditions
Explore the condition pages connected to this study.