Jun 11, 2024 · The International 22q11.2 Foundation is a nonprofit organization dedicated to supporting the needs of families and individuals affected by ...

2 Deletion syndrome or 22q (also referred to as Velocardiofacialsyndrome ... This tiny missing portion of chromosome 22 can affect every system in the human body.

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 conceived. The ...

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 ...

May 9, 2024 · The major clinical manifestations of 22q11.2DS include congenital heart disease, particularly conotruncal malformations (ventricular septal ...

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

Duration: 2:30
Posted: Nov 12, 2014