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.

Über den Inhalt der Website

Alle Informationen auf dieser WebSite dienen ausschließlich der Aufklärung. Der richtige Ort, um spezifischen medizinischen Rat, Diagnosen und Behandlungen zu erhalten, ist Ihr Arzt. Die Nutzung dieser Website erfolgt ausschließlich auf eigene Gefahr. Wenn Sie etwas finden, das Ihrer Meinung nach einer Korrektur oder Klärung bedarf, lassen Sie es uns bitte wissen: 

Senden Sie eine E-Mail: info@cdlsWorld.org