|Other names||DiGeorge anomaly, velocardiofacial syndrome (VCFS), Shprintzen syndrome, conotruncal anomaly face syndrome (CTAF), Takao syndrome, Sedlackova syndrome, Cayler cardiofacial syndrome, CATCH22, 22q11.2 deletion syndrome|
|A child with DiGeorge syndrome|
|Symptoms||Variable; commonly congenital heart problems, specific facial features, cleft palate|
|Complications||Kidney problems, hearing loss, autoimmune disorders|
|Causes||Genetic (typically new mutation)|
|Diagnostic method||Based on symptoms and genetic testing|
|Differential diagnosis||Smith-Lemli-Opitz syndrome, Alagille syndrome, VACTERL, Oculo-auriculo-vertebral spectrum|
|Treatment||Involves many healthcare specialties|
|Prognosis||Depends on the specific symptoms|
|Frequency||1 in 4,000|
The symptoms often include congenital heart problems, facial features, infections, developmental delay, learning problems and cleft palate. Other conditions include kidney problems, hearing loss and autoimmune disorders such as rheumatoid arthritis or Graves disease.
DiGeorge syndrome is due to the deletion of 30 to 40 genes in the middle of chromosome 22 at a location known as 22q11.2. About 90% of cases occur due to a new mutation during early development, while 10% are inherited from a person's parents.
Although there is no cure, treatment can improve symptoms. This often includes efforts to improve the function of the many organ systems involved. Long-term outcomes depend on the symptoms present and the severity of the heart and immune system problems. With treatment, life expectancy may be normal.
DiGeorge syndrome occurs in about 1 in 4,000 people. The syndrome was first described in 1968 by American physician Angelo DiGeorge. In late 1981, the underlying genetics were determined.
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|Wikimedia Commons has media related to DiGeorge syndrome.|
- DiGeorge syndrome at the Open Directory Project
- McDonald-McGinn DM, Emanuel BS, Zackai EH (December 16, 2005). "22q11.2 Deletion Syndrome". In Pagon RA, Bird TD, Dolan CR, Stephens K (eds.). GeneReviews. PMID 20301696. NBK1523.
- Firth HV (February 17, 2009). "22q11.2 Duplication". In Pagon RA, Bird TD, Dolan CR, Stephens K (eds.). GeneReviews. PMID 20301749. NBK3823.