NIH study explores rare genetic conditions in kids to boost research skills
NCT ID NCT02769949
First seen Nov 01, 2025 · Last updated May 06, 2026 · Updated 27 times
Summary
This study enrolled 96 children with known or suspected genetic disorders, including conditions like autism and Fragile X syndrome. The main goal was to give clinic staff hands-on experience and explore new research methods, not to provide treatment. Participants had medical exams, lab tests, and imaging, and some family members gave DNA samples.
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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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National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
Conditions
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