DiGeorge syndrome/chromosome 22q11.2 deletion syndrome

Curr Allergy Asthma Rep. 2001 Sep;1(5):438-44. doi: 10.1007/s11882-001-0029-z.

Abstract

DiGeorge syndrome is characterized by conotruncal cardiac defects, hypocalcemia, and a hypoplastic thymus. Many, but not all, patients have a heterozygous deletion of chromosome 22q11.2. In its most severe form, it represents a devastating syndrome with high mortality. Patients with severe immunodeficiency are candidates for a thymic transplant or a fully matched bone marrow transplant. Fortunately, the majority of patients with either DiGeorge syndrome or chromosome 22q11.2 deletion syndrome have a mild to moderate immunodeficiency. These patients may develop recurrent infections or autoimmune disease.

Publication types

  • Review

MeSH terms

  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22* / immunology
  • DiGeorge Syndrome / epidemiology
  • DiGeorge Syndrome / immunology*
  • DiGeorge Syndrome / therapy
  • Humans
  • Immunologic Deficiency Syndromes / epidemiology
  • Immunologic Deficiency Syndromes / immunology
  • Immunologic Deficiency Syndromes / therapy