Why should you sign up?

We all got involved with Cornelia de Lange syndrome for different reasons; we have CdLS, we are parents, we are brothers or sisters, we are family or friend, we are caring for a person with CdLS, we are doctors, we are teachers, we are researchers, we are curious...
And because we are this we understand the importance of sharing our experience!

You will have something to share as well, maybe just that you are 'involved'... but by seeing (reading), talking (writing), learning and sharing we will make life with CdLS more beautiful, that is our dream.

So please signup for our online community, it is free

Become a member!
Maybe you already signed-up, do not signup twice, login by clicking here!

About the website contents


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@rtsyndroom.nl