Bergamo gene discovery may explain kidney disease patterns
NCT ID NCT06594367
First seen Nov 01, 2025 · Last updated May 23, 2026 · Updated 25 times
Summary
This study looked at 10 people with a kidney disease called ADPKD to see if a specific gene change (a deletion in the PKD2 gene) is common in families from the Bergamo area. Researchers interviewed participants about their health and family history to understand how this gene change affects the disease. The goal was to learn more about the link between genetics and symptoms, not to test a new treatment.
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 AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE (ADPKD 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
-
Clinical Research Centre for Rare Diseases Aldo e Cele Daccò
Ranica, BG, 24020, Italy
Conditions
Explore the condition pages connected to this study.