Cornelia de Lange Syndrome is a very rare condition. The Foundation staff and volunteers are often asked questions about CdLS. These are some of the most common ones.
What does the word syndrome mean?
What are the features that go together to make Cornelia de Lange Syndrome?
Why is it called Cornelia de Lange Syndrome?
Are there other names for the syndrome?
Are there different types of Cornelia de Lange Syndrome?
How common is the syndrome?
What are the Main Features of the Syndrome?
Are there other problems that are commonly seen in the syndrome?
Are there any treatments or therapies that will help my child?
What does the future hold for my child?
Why does my child have Cornelia de Lange Syndrome and could I have another child with Cornelia de Lange Syndrome?
Can the syndrome be diagnosed before birth?
Is there any research being carried out on the syndrome?
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