22q11.2 deletion syndrome is a disease seen at birth that affects many parts of the body. It is rare.
It is linked to groups of syndromes. The most common types are DiGeorge syndrome and velocardiofacial syndrome.
22q11.2 deletion syndrome is caused by missing genes in chromosome 22q11.2.
The risk of this problem is higher in babies who have other family members who have it.
Problems differ among children. The missing genes can result in problems in almost any part of the body. A child may have:
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The doctor may suspect 22q11.2 deletion syndrome at birth in a child that has certain features or health issues.
The doctor may ask about your child's symptoms and health history. A physical exam will be done.
A genetic test can be done to confirm the diagnosis. Other tests may be:
There is no cure. The goal is to manage health problems. How it is done depends on the problems that a child has. Some choices are:
There are no guidelines to prevent this health problem.
Immune Deficiency Foundation
National Center for Biotechnology Information
Canadian Association of Genetic Counsellors
22q11.2 deletion syndrome. EBSCO DynaMed website. Available at: https://www.dynamed.com/condition/22q11-2-deletion-syndrome. Accessed November 2, 2020.
22q11.2 deletion syndrome. Stanford Children's Health website. Available at: http://www.stanfordchildrens.org/en/topic/default?id=22q112-deletion-syndrome-90-P01682. Accessed November 2, 2020.
McDonald-McGinn DM, Sullivan KE, et al. 22q11.2 deletion syndrome. Nat Rev Dis Primers. 2015 Nov 19;1:15071.
What is 22q11.2 deletion syndrome? Nationwide Children's website. Available at: http://www.nationwidechildrens.org/22q-signs-and-symptoms. Accessed November 2, 2020.
Last reviewed September 2020 by EBSCO Medical Review Board Kari Kassir, MD Last Updated: 5/5/2021