Welcome, please tell us more


Thank you for your interest in the Cornelia de Lange syndrome (CdLS). The Website you have just registered on is meant to help and inform about this rare syndrome.

We would like that this website helps you well and to serve you best we would like to, kindly, ask you the following;

  1. If you would like to ask questions to one of the CdLS Experts some more information about the person with CdLS (if appropiate) is needed by the experts,
  2. If you would like to join one of the associations of the world federation some more detailed contact information is required,
  3. If you would like us to contact you more personally (this email is generated by the website) please mark this in your personal settings, likewise if you like to be contacted by others so you can share stories and experiences.

If you want you can login and fill in this information by going to;
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This page contains 4 sections (tabs); Profile, Preferences, CdLS Info and CdLS Person. (We continuously try to improve the website, so let us know if something is not clear or if you have an idea for improvement!!)

(This email is generated by the website, it might well be that you have already contacted a CdLS organization, still we would greatly appreciate if you would complete some details, other wise our apologies for asking twice!)

For each section we will show you a screenshot of what and how you can complete that section.

À propos du contenu du site Web

Toutes les informations contenues dans ce site Web sont uniquement destinées à des fins éducatives. Pour obtenir des conseils, des diagnostics et des traitements médicaux spécifiques, adressez-vous à votre médecin. L'utilisation de ce site est strictement à vos propres risques. Si vous trouvez quelque chose qui, selon vous, nécessite une correction ou une clarification, veuillez nous en faire part à l'adresse suivante : 

Envoyez un courriel : info@cdlsWorld.org