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Velo-Cardio-Facial Syndrome

This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site.

Velo-Cardio-Facial Syndrome Educational Foundation, Inc.

National network. Founded 1996. Support and resource network for families coping with velo-cardio-facial syndrome (aka Shprintzen syndrome, 22q11 deletion syndrome, 22q11.2 deletion syndrome and DiGeorge syndrome). Provides family programs, parent-to-parent networking, educational materials, newsletter and annual conference.
Write:
Velo-Cardio-Facial Sydrome Ed. Fdn
P.O. Box 12591
Dallas, TX 75225
Voice: 855-800-8237
Website: http://www.vcfsef.org
E-mail: info@vcfsef.org
Verified: 1/15/2013

WebMD Medical Reference from the American Self-Help Clearinghouse

Last Updated: February 25, 2014
This information is provided as a resource and does not constitute an endorsement for any group.  It is the responsibility of the reader to decide whether a group is appropriate for his/her needs.  For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site.This information is not intended to replace the advice of a doctor. Healthwise disclaims any liability for the decisions you make based on this information.   

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