Global hunt for clues about Ultra-Rare brain disorder
NCT ID NCT07372833
Summary
This study aims to map the natural progression of CAMK2-related neurodevelopmental disorders, which are extremely rare genetic conditions affecting brain development. Researchers will collect detailed information from 150 children and adults worldwide who have specific CAMK2 gene mutations. The goal is to better understand how these disorders develop over time and identify patterns that could improve care and guide future treatment research.
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Contacts and locations
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Study contacts
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Contact
Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Erasmus MC
RECRUITINGRotterdam, South Holland, 3015 GD, Netherlands
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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