22q Deletion Velocardiofacial At a Glance
picture courtesy of Dani and her family
Print a PDF of all the 22q deletion syndrome information.
The GEMSS website is intended primarily for educators and families of preschool through elementary school age children. While much of the information may also apply to older children, the authors are aware that there is a lack of information about transition issues that would be helpful for older children and young adults. It is our hope that this information can be added in the future.
22q Deletion Velocardiofacial syndrome is a genetic condition caused by a very tiny missing piece on chromosome 22. This condition is highly variable in its severity and in the number of body systems that are affected. There is a difference in severity even between affected individuals in the same family. The most commonly affected areas are the heart, the palate (roof of the mouth) and speech, learning and behavior.
About one in every 4 - 6,000 babies is born with 22q deletion syndrome. Children with 22q deletion may have distinct facial features.
Other names for 22q deletion syndrome include:
Click here to read about the symptoms that can be associated with the syndrome.
- 22q11.2 deletion syndrome
- DiGeorge syndrome
- Velocardiofacial syndrome
- Shprintzen syndrome
- Conotruncal anomaly face syndrome
- Caylor cardiofacial syndrome
- Autosomal Dominant Opitz G/BBB syndrome.