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Diseases

Genetic and Rare Diseases Information Center (GARD)

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22q11.2 deletion syndrome


Other Names for this Disease

  • Autosomal dominant Opitz G/BBB syndrome
  • CATCH22
  • Cayler cardiofacial syndrome
  • Chromosome 22q11.2 deletion syndrome
  • Conotruncal anomaly face syndrome
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Organizations

Organizations Supporting this Disease

  • Chromosome 22 Central - US Office
    Murney Rinholm
    7108 Partinwood Drive
    Fuquay-Varina, NC 27526
    Telephone: 919-567-8167
    E-mail: murney.rinholm@c22c.org
    Website: http://www.c22c.org

  • Chromosome Disorder Outreach
    PO Box 724
    Boca Raton, FL 33429
    Telephone: 561-395-4252
    E-mail: info@chromodisorder.org
    Website: http://www.chromodisorder.org

  • International DiGeorge / VCF Support Network
    c/o Family Vooices of New York
    46 1/2 Clinton Avenue
    Cortland, NY 13045
    Telephone: 607-753-1621 (day); 607-753-1250 (evening)
    Fax: 607-758-7420

  • The 22q11 Group
    PO Box 1302
    Milton Keynes MK13 0LZ
    United Kingdom
    Telephone: +44 1908 320 852
    E-mail: 22q11@melcom.cix.co.uk

  • The International 22q11.2 Deletion Syndrome Foundation, Inc.
    22 Tanforan Court
    Matawan, NJ 07747
    Telephone: 877-739-1849
    E-mail: i22qdsf@gmail.com
    Website: http://www.22q.org

  • Unique – Rare Chromosome Disorder Support Group
    P.O. Box 2189
    Caterham
    Surrey CR3 5GN
    United Kingdom
    Telephone: 440 1883 330766
    E-mail: info@rarechromo.org
    Website: http://www.rarechromo.org

  • Velo-Cardio-Facial Syndrome Educational Foundation
    PO Box 874
    Milltown, NJ 08850
    Toll-free: 866-VCFSEF5
    Telephone: 732-238-8803
    E-mail: info@vcfsef.org
    Website: http://www.vcfsef.org

Social Networking Websites

  • DNAandU.org is a Web site and blog that collects firsthand stories from people facing issues, making tough decisions, and using genomic (DNA) information in their own healthcare. Click on the link to learn from their experiences and/or submit your own story.
  • RareShare is an online social hub dedicated to patients, families and healthcare professionals affected by rare medical disorders.

Organizations Providing General Support

Other Names for this Disease
  • Autosomal dominant Opitz G/BBB syndrome
  • CATCH22
  • Cayler cardiofacial syndrome
  • Chromosome 22q11.2 deletion syndrome
  • Conotruncal anomaly face syndrome
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.