2 Foundation is a nonprofit organization dedicated to supporting the needs of families and individuals affected by chromosome 22q11.2 differences by promoting ...

22q11.2 Deletion syndrome or 22q (also referred to as Velocardiofacialsyndrome (VCFS), and/or DiGeorge syndrome) is a disorder caused by a small missing ...

The 22q11.2 deletion syndrome is a genetic disorder caused by a missing section (microdeletion) of chromosome 22, which is present from the time a child is ...

The major clinical manifestations of 22q11.2DS include congenital heart disease, particularly conotruncal malformations (ventricular septal defect, tetralogy of ...

Jan 13, 2024 · This condition is due to missing part of chromosome 22. It may cause heart issues, thyroid problems, cleft palate, lower immunity and other ...

22q11.2 Society is a UK registered charity supporting families affected by DiGeorge syndrome, VCFS and 22q11.2 deletion.

What is 22q11.2 Deletion? How Common is 22q Deletion? Is 22q11.2 Deletion the same as DiGeorge syndrome? Is 22q Deletion Hereditary? What are the symptoms? How ...

What is 22q? · 22q For Teachers · Our Team · 22q Family Map

Dec 1, 2019 · The deletion occurs near the middle of the chromosome at a location designated q11.2. 22q11.2 deletion syndrome has many possible signs and ...