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9. Diagnosing DiGeorge Syndrome

Diagnosis is confirmed by a blood test to detect the genetic deletion in chromosome 22. A doctor will order this test if the child shows multiple signs and symptoms of DiGeorge syndrome. Sometimes, a heart defect can be enough to prompt the test, because this is such a common sign of the syndrome. In some cases, the lab may not confirm DiGeorge syndrome despite the indicative symptoms. Treatment will proceed in a similar manner, regardless.

Blood Test Diagnosis fotografixx / Getty Images

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