Scientists launch study to unlock secrets of rare bone diseases
NCT ID NCT05031507
First seen Nov 19, 2025 · Last updated May 16, 2026 · Updated 33 times
Summary
This study aims to gather information about rare skeletal disorders that are not well understood. Researchers will collect medical records, blood and tissue samples, and imaging from 100 participants aged 2 months and older, including healthy family members. The goal is to find genetic causes and track how these conditions change over time. No treatments or cures are being tested.
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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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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: •••••@•••••
Conditions
Explore the condition pages connected to this study.