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

22q (also referred to as Velocardiofacialsyndrome (VCFS), and/or DiGeorge syndrome) is a disorder caused by a small missing piece of the 22nd chromosome.

Dec 1, 2019 · 22q11.2 deletion syndrome (which is also known by several other names, listed below) is a disorder caused by the deletion of a small piece of chromosome 22.

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 ...

22q11.2 Deletion Syndrome · 22q For Teachers · Our Team · 22q Family Map

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 ...

Nov 19, 2015 · 22q11.2 deletion syndrome (22q11.2DS) is the most common chromosomal microdeletion disorder, estimated to result mainly from de novo ...

Aug 23, 2018 · 22q11.2, or 22q for short. Also called DiGeorge syndrome, this condition is caused by the deletion of a piece of chromosome 22.

Dec 13, 2023 · 22q11.2 is DiGeorge syndrome. It has noticeable features, one of which being cardiac defects. A common cardiac defect with that syndrome is tetralogy of fallot.