Massive newborn study hunts for hidden rare diseases
NCT ID NCT04393701
Summary
This study aims to screen about 100,000 newborns in the Normandy region of France for two rare genetic disorders called MPS I and Pompe disease. Researchers will use a simple blood spot test collected shortly after birth to see how common these conditions are in the population. The goal is to improve early detection so that babies can get treatment sooner if needed.
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 NEONATAL SCREENING 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
Study contacts
-
Contact
Phone: •••-•••-•••• Email: •••••@•••••
-
Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
-
Caen University Hospital
RECRUITINGCaen, France
Contact
-
Rouen University Hospital
RECRUITINGRouen, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
Explore the condition pages connected to this study.