Massive study aims to unlock secrets of rare inherited nerve diseases
NCT ID NCT00004568
First seen Nov 01, 2025 · Last updated May 03, 2026 · Updated 32 times
Summary
This study looks at people with inherited neurological disorders to learn how these diseases develop and change over time. Researchers will collect medical history, do physical exams, and take blood or skin samples for genetic testing. Up to 3,500 children and adults with these rare conditions can join. The goal is to better understand the diseases, not to test a new 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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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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National Institutes of Health Clinical Center
RECRUITINGBethesda, Maryland, 20892, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
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University of Mali
COMPLETEDBamako, Mali
Conditions
Explore the condition pages connected to this study.