Scientists track rare disorder to unlock its secrets
NCT ID NCT00013559
Summary
This study aims to learn more about Smith-Magenis syndrome (SMS), a rare genetic disorder, by observing how it affects people over time. Researchers will follow nearly 600 participants of all ages with SMS, conducting various medical, developmental, and behavioral tests during visits to the NIH. The goal is to create a detailed picture of the condition to help guide future care and research, not to test a new treatment.
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.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for SMITH-MAGENIS SYNDROME (SMS) are added.
By submitting, you agree to our Terms of use
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Locations
-
National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
Conditions
Explore the condition pages connected to this study.