22q11.2 Deletion Syndrome

(Included conditions:  DiGeorge syndrome, Velocardiofacial syndrome, Conotruncal anomaly face syndrome, Autosomal dominant Opitz G/BBB syndrome, Sedlackova syndrome, Cayler cardiofacial syndrome)

If you have just found out through prenatal testing that your baby has or may have 22q11.2 deletion syndrome and are looking for more information, the Genetic Support Foundation is a good starting point.

There are many other important resources out there, including your doctor and genetic counselor. We have also compiled a list of resources that can provide you with additional information and support. After reviewing the information below, if you have a question that you are having difficulty finding an answer for, please feel free to contact us.