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The Cornelia de Lange Syndrome (CdLS) Foundation (USA) provides a host of services for anyone touched by this little-known genetic syndrome and other isolating conditions. Learn more about us, visit cdlsusa.org
The CdLS USA Foundation Adult Transition, published on 1 Dec 2019
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
info@cdlsworld.org
