Thanks to working together worldwide we were able to collect a lot of useful information and experiences about the Cornelia de Lange syndrome. After many researches, articles and stories down our road we have collected all of this on this platform.
coming soon ...
All of the information on this WebSite is for education purposes only. The place to get specific medical advice, diagnoses, and treatment is your doctor. Use of this site is strictly at your own risk. If you find something that you think needs correction or clarification, please let us know at:
Send a email: info@cdlsWorld.org
vereniging@cdlsworld.org
