Scientists hunt clues to predict rare childhood tumor risk
NCT ID NCT00780117
Summary
This study aimed to understand why some people with Currarino syndrome develop tumors while others don't. Researchers followed 57 patients for several years, collecting genetic information, MRI scans, and blood tests. The goal was to identify markers that could predict which patients are at highest risk for tumor development or cancer transformation.
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 SACROCOCCYGEAL TERATOMA are added.
Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
Genom att skicka in godkänner du våra Användarvillkor
Locations
-
Hôpital Necker-Enfants Malades Pediatric Surgery Department
Paris, 75015, France
Conditions
Explore the condition pages connected to this study.