Scientists hunt for genetic clues behind rare lung malformation
NCT ID NCT01732185
First seen Nov 01, 2025 · Last updated Jun 16, 2026 · Updated 31 times
Summary
This study looked at tissue samples from 45 children under 8 who had surgery for a rare lung condition called CCAM. The goal was to find genetic and molecular changes that might cause the malformation. Researchers analyzed gene activity and protein patterns to better understand the disease.
Disclaimer
Read more
Show less
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.
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 CONGENITAL CYSTIC ADENOMATOID MALFORMATION (CCAM) 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
-
Necker-Enfants Malades Hospital
Paris, 75015, France
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.