Velocardiofacial Syndrome (VCFS)
Follow the links below to learn more about specific conditions. This is by no means a complete database of craniofacial anomalies or treatments. If you require information not found here, please contact us. Submit links for additional resources to the webmaster. Back to list of Conditions.
National organization founded by parents
Family support network at Yahoo
At Children's Hospital of Philadelphia (CHOP)
Regional organization founded by parents
Authored by Robert Ardinger, Jr, MD and Holly Ardinger, MD
Executive Director, Dr. Robert J. Shprintzen
A list of anomalies which have been found in VCFS
From the National Craniofacial Association
In Children with Chromosome 22q11.2 Deletion Syndrome
From University of Kansas Medical Center
From Stanford University
Fact sheet from the National Institute on Deafness
The 22q11 Group
Listed by state
Country-by-country information
Edited by James N. Parker and Philip M. Parker
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