Resources- Specific Diagnosis Card Catalog- Carbohydrate-Deficient Glycoprotein Syndrome


  • Who to Contact
  • Where to Go to Chat with Others?
  • Personal Accounts
  • Learn More About it
  • Links
  • Who to Contact

    CDG Family Network Foundation
    P.O. Box 149
    Anamoose, ND 58710
    1-903-640-5273
    E-mail: cdgaware@aol.com
    Web: www.cdgs.com

    Support for parents of children diagnosed with congenital disorders of glycosylation, an inherited metabolic disease affecting all body parts, especially the central and peripheral nervous systems. Support is attained primarily online, but forum also provides information and referrals, biannual newsletter, phone support, advocacy. Bulletin board for families to interact with questions, comments and updates.

    Where to go to Chat with Others?

    CDG List
    This list was started for parents and professionals who have children/patients with this condition. Parents of children with CDG or related diseases are invited to share your experiences as well as questions and answers from other families with the same concerns.

    Personal Accounts

    "Our Stories"

    Learn More About It

    What is a Congenital Disorder of Glycosylation?

    The C D G - Syndrome, what is that?

    Carbohydrate-Deficient Glycoprotein Type I; CDG1 information from OMIM

    Carbohydrate-Deficient Glycoprotein Type II information from OMIM

    Carbohydrate-Deficient Glycoprotein Type III information from OMIM

    Carbohydrate-Deficient Glycoprotein Type IV information from OMIM

    Links

    CDGS Family Network

    The CDG Society - Sweden

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