Scientists seek clues in rare bone disorder
NCT ID NCT05368064
Summary
This research aims to learn more about cleidocranial dysplasia (CCD), a rare genetic condition affecting bone and tooth development. The study will enroll 300 people with CCD to examine their genes, document their symptoms, and understand how the condition affects their daily life and finances. The goal is to gather information to help improve diagnosis and care for people with CCD in the future.
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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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