Rare bone disorder study seeks to unlock genetic secrets and improve lives
NCT ID NCT05368064
First seen Nov 01, 2025 · Last updated Apr 30, 2026 · Updated 26 times
Summary
This study looks at Cleidocranial Dysplasia (CCD), a rare genetic condition affecting bones and teeth. Researchers will collect medical history, quality-of-life surveys, and DNA samples from 300 participants to better understand the disease and improve care. The goal is to help doctors diagnose and treat CCD more effectively.
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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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Locations
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Johns Hopkins University
Baltimore, Maryland, 21205, United States
Conditions
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