Scientists track kids with rare gene to unlock cancer clues
NCT ID NCT06805734
Summary
This study aims to better understand the health risks, especially cancer risk, in children who have a specific change in their PTEN gene. Researchers will follow 50 children and some of their affected family members in Italy for 5 years, performing regular check-ups and scans. The goal is to gather detailed information to create better future health monitoring guidelines for these children.
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 PTEN HAMARTOMA SYNDROME 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
-
Fondazione IRCCS Istituto Neurologico Carlo Besta
RECRUITINGMilan, 20133, Italy
Contact
Contact
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
Explore the condition pages connected to this study.