22q11.2 Deletion Syndrome

22q11.2 Deletion Syndrome - What is it for

22q11.2 deletion syndrome (22q11.2DS) is a genetic disorder that can affect many parts of the body, including the heart, immune system and development.

It may present at birth, in childhood or older. Common symptoms include congenital heart defects, palatal abnormalities, an impaired immune system, characteristic facial features and learning difficulties, but these vary widely.

How common is 22q11.2DS?

About one in 6,000 people are born with 22q11.2DS. Occurrences of 22q11.2DS are present across all racial groups and it affects both genders equally.

22q11.2 Deletion Syndrome - How to prevent?

22q11.2 Deletion Syndrome - Preparing for surgery

22q11.2 Deletion Syndrome - Post-surgery care

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Article contributed by SingHealth Duke-NUS Genomic Medicine Centre

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22q11.2 Deletion Syndrome

22q11.2 Deletion Syndrome - What is it for

How common is 22q11.2DS?

22q11.2 Deletion Syndrome - How to prevent?

22q11.2 Deletion Syndrome - Preparing for surgery

22q11.2 Deletion Syndrome - Post-surgery care

Our Breast Team

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Prof Ivy Ng

SingHealth GCEO

22q11.2 Deletion Syndrome

22q11.2 Deletion Syndrome - What is it for

How common is 22q11.2DS?

22q11.2 Deletion Syndrome - How to prevent?

22q11.2 Deletion Syndrome - Preparing for surgery

22q11.2 Deletion Syndrome - Post-surgery care

Our Breast Team

Filter: By designation or sub-specialty

Related Conditions

Prof Ivy Ng

SingHealth GCEO