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DiGeorge Syndrome / 22q11.2 Deletion Syndrome / CATCH 22 Syndrome

DiGeorge Syndrome - Frequently Asked Questions

Q: Which doctor should I consult for DiGeorge syndrome?

A: The neonatologist attending to your baby will identify the syndrome soon after birth. If diagnosis is not possible immediately, then consult a pediatrician at follow-up.

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Q: When should I consult a pediatrician?

A: You should visit a pediatrician as soon as you see symptoms such as a severe heart defect, cleft palate or a combination of other factors typical of DiGeorge syndrome.

Q: What are the chances that my next child will be born with DiGeorge syndrome?

A: If neither of the parents have the condition, then the chance is 1 in 100 (1%). However, if either of the parents have the condition, then the chance increases to 1 in 2 (50%).

Q: What are the chances of survival of children suffering from DiGeorge syndrome?

A: The mortality rate of children suffering from DiGeorge syndrome is 4%, and most survive into adulthood.

Q: Can DiGeorge syndrome be prevented?

A: No. However, the symptoms can be controlled by proper treatment.


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