Scientists test new way to track walking issues in rare genetic disorders
NCT ID NCT05161494
First seen May 08, 2026 · Last updated May 08, 2026
Summary
This study tested a method to measure walking problems in 41 people aged 6 and older with rare genetic diseases like Tuberous Sclerosis Complex and STXBP1-related epilepsy. Participants walked in a special lab with cameras to track their movements. The goal was to see if this approach could reliably detect gait issues, not to provide treatment.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Locations
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University of Antwerp
Antwerp, 2160, Belgium
Conditions
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