DiGeorge syndrome/velocardiofacial syndrome: the chromosome 22q11.2 deletion syndrome

Adv Exp Med Biol. 2007:601:37-49. doi: 10.1007/978-0-387-72005-0_4.

Abstract

Chromosome 22q11.2 deletion (CH22qD) syndrome is also known as DiGeorge syndrome or velocardiofacial syndrome. This deletion syndrome is extremely common with nearly one in 4000 children being affected. Recent advances and a holistic approach to patients have improved the care and well-being of these patients. This review will summarize advances in understanding the health needs and immune system of patients with CH22qD syndrome. Patients will most often need interventions directed at maximizing function for many organ systems but can ultimately have a high level of functioning.

Publication types

  • Review

MeSH terms

  • Adolescent
  • Adult
  • Allergy and Immunology
  • Child
  • Child, Preschool
  • Chromosome Deletion
  • Chromosomes, Human, Pair 22*
  • DiGeorge Syndrome / diagnosis*
  • DiGeorge Syndrome / genetics*
  • DiGeorge Syndrome / immunology
  • Gene Deletion*
  • Humans
  • Infant
  • Infant, Newborn
  • Models, Genetic