Having a child with DiGeorge syndrome is challenging. You must deal with numerous treatment issues, manage your own expectations and meet the needs of your child. Organizations such as the Velo-Cardio-Facial Syndrome Educational Foundation provide educational materials, support groups and other resources for parents of children with DiGeorge syndrome.
Sept. 03, 2014
- DiGeorge syndrome. Immune Deficiency Foundation. http://primaryimmune.org/about-primary-immunodeficiencies/specific-disease-types/digeorge-syndrome/. Accessed June 16, 2014.
- 22q11.2 deletion syndrome. Genetics Home Reference. http://ghr.nlm.nih.gov/condition/22q112-deletion-syndrome. Accessed June 16, 2014.
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- Chromosome 22q11.2 deletion syndrome. National Organization for Rare Disorders. http://www.rarediseases.org/rare-disease-information/rare-diseases/byID/853/viewFullReport. Accessed June 16, 2014.
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- Hofstetter AM, et al. Live vaccine use and safety in DiGeorge syndrome. Pediatrics. 2014;133:e946.
- VCFSEF support groups & contacts in the United States. Velo-Cardio-Facial Syndrome Educational Foundation, Inc. http://www.vcfsef.org/sub_page.php?sub_id=27&parent_id=2. Accessed June 17, 2014.
- Babovic-Vuksanovic D (expert opinion). Mayo Clinic, Rochester, Minn. Aug. 3, 2014.
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