
Cornelia de Lange Syndrome Foundation, Inc.
Cornelia de Lange Syndrome, promoting research & providing support to individuals with CdLS & their families 860.676.8166 #raredisease #cdlsawareness This page is where people can connect with each other and the CdLS Foundation staff. The Cornelia de Lange Syndrome (CdLS) Foundation is a family support organization which exists to ensure early and accurate diagnosis of CdLS, promote research into the casues and manifestations of the syndrome, and help people with a diagnosis of CdLS and others with similar characteristics make informed decisions throughout their lives. Reaching Out, Providing Help and Giving Hope.

Founded
1981
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1083
Traffic
3720803
Home | CdLS Foundation Establish Community. Educate Families. Enable Advocacy. The Cornelia de Lange Syndrome CdLS Foundation provides a host of services for anyone touched by this littleknown genetic syndrome and other isolating conditions.
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